Methamphetamine synthesis from P2P by NaBH4 reduction. Medium-Scale.

[btcboss2022]

Introduction.​

I represent to BB audience Methamphetamine synthesis method of 1-phenyl-2-propanon (P2P) reduction by NaBH4. Following method allows obtaining and large batches of product. The hardest problem of this method is the heat generating during exothermic reaction of imine reduction. Extremely important keep temperature in described frames and keep all reagent and reaction atmosphere dry (use drying tubes with CaCl2). Also, manipulations with NaBH4 is quite dangerous and take a lot of attention because this reagent has toxic effects, reacts with water and alcohols with releasing enormous amount of hydrogen and form the corresponding borate, it may cause an explosion, burns and injuries. You have to use chemical glass, gloves, chemical coat and respirator.​

Equipment and glassware:​

• Ceramic mortar;​
• 2 L (x2), 0.5 L (x2) and 200 ml (x2) beakers;​
• 2 L (x2) and 10 L Erlenmeyer flask;​
• Measuring cylinder for 100 ml;​
• 2 L three-necked round bottom flask with plugs;​
• 2 L round bottom flask with vacuum quickfit or Schlenk flask;​
• 0.5 L Simple dropping funnel with Claisen flask and drying tube or 0.5 L equal pressure dropping funnel;​
• 1 L Separator funnel;​
• 2 L Evaporation flask;​
• Pyrex dish 0.5 L;​
• Magnetic stirrer with heating plate;​
• Retort stand and clamp for securing apparatus;​
• Silicone-oil bath;​
• Icecubes/methanol bath (-10 °C) or Mashed ice with salt (-10 °C);​
• Laboratory scale (1 g-1 kg is suitable);​
• Oven;​
• Laboratory grade thermometer (-20 °C to 200 °C) with three-necked flask adapter;​
• Aspirator;​
• HCl laboratory generator;​
• Drying tube x2;​
• Rotavap machine with water bath;​
• Filter paper.​

Reagents:​

• 138 gram P2P (1 mole) (1-phenyl-2-propanone);​
• 10% Methylamine in Methanol (w/w) - 1000 ml with 100 g MeNH2 (~3 moles);​
• Magnesium Sulfate - 36 g (MgSO4·7H2O, oven dry at 300 °C for 2h MgSO4·1H2O) [For drying MeOH/MeNH2 solution];​
• Silica Gel (3-5 mm balls) - 200 ml (dry at 300 °C/2h, they will darken!) [For absorbing 2 mol H2O during rxn];​
• 15 gram NaBH4 as a reducing agent for the formed (water-free!) imine;​
• 5-7 L distilled water + ~5 L distilled water to filling rotavap machine bath;​
• 1 L Dichloromethane (DCM);​
• 0.5 L Acetone.​

Important: the reaction is very sensitive to any water (fluid or vapour in the air!).

Note: hold all manipulations in pull out probe or under exhaust hood; methylamine is a rather toxic substance, do not let its vapors enter the respiratory tract. Using respiratory mask is required. Inhalation of methylamine causes severe skin irritation, eyes and upper respiratory tract. Firstly, leads to excitement and then to depression of the central nervous system. Death can occur from respiratory arrest.​

Procedure.​

Precursors drying.
First quickly crunch your pre-dried (oven, 300 °C, 3 hrs.) dry MgSO4 to pop corn shaped rocks in a mortar, sieve the powder out, and directly put the rocks under max. mixing in the Methanol/Methylamine mix (1000 ml) and close the pot to let no water from the air in. Keep mixing for 10 minutes, then all the water will be taken up to the MgSO4. Let stand and wait till all the MgSO4 is on the bottom. Now quickly tap off the now dry MeOH/methylamine (MA) mix in a 2 L three-necked round bottom flask and close that one. Wash directly your empty pot with lots of water, to remove the smell of methylamine, so you can safely store it.
​

Synthesis.

Now add the 200 ml (measure in beaker, neglect the free spaces) dry Silicagel beads (2-5 mm) and a magnetic mixer bar also in the 2 L flask and close again. Keep 2 L flask in Silicone-oil bath at 20 °C. Silicone-oil only slowly warms up! Do not apply heat now, it's only meant as a cooling medium in this stage. Now add slowly via a dropping funnel the 138 g P2P to the 2 L flask under strong mixing. The temperature rises to 23 °C during the (water-free) Imine forming. The water from this reaction is taken up by the dried Silicagel! This takes 30 minutes. Let, then mix for another hour. The reaction mix color changes from light yellow to coffee+milk color. Temp 23 °C.​

View attachment 2944 ​

Stop mixing after this 1 hour and pour the fluid off into a 2 L glass erlenmeyer with flat bottom and add a mixbar. The remaining Silicagel is washed 3 times with 50 ml dried (use silicagel) methanol, to catch the remaining Imine, and those 2 x 50 ml is also poured into the 2 L erlenmeyer. Now put the 2 L erlenmeier on magn.mixer, in an icecubes/methanol bath (-10 °C) (or mashed ice with salt) and start strong mixing. Put a drip funnel on top of 2 L erlenmeier, in rubber ring. Now start adding, every 5 min., a teaspoonfull (flat off!) of NaBH4 in minimum methanol, wash it from funnel with minimum methanol amount. After every spoonfull, stopper the funnel loosely with a rubber stopper. This takes 2.5 hrs. Do not exceed a temp of more than 20 °C! You can add the next spoon at ±8 °C. Solution color is light clear orange/brown. Let mix in total for 8.5 h (could perhaps be lot fewer hours).​

View attachment 2945 ​

The total volume is ~1900 ml. Add then the mix to 5 L distilled water into a 10 L flask, under magn.mixing. The pH=12. Add then 500 ml DiChloroMethane (DCM) and mix strongly for 30 min. Let oil precipitate and a dark, honey-coloured layer of DCM+oil settle onto the bottom. Decant the water part with an aspirator + siliconetube. Fill the rest (water+DCM+oil) in a seperatory funnel and tap off only the DCM+oil = 550 ml. (DCM b.p. 40 °C). The leftover MgSO4 and boro salts stayed nicely in the waterpart. Then dry the DCM+oil with some dry MgSO4 and decant in 2l erlenmeier. Wash this MgSO4 with some fresh, DRY DCM and add the DCM washings to the now dry DCM+oil. Total volume DCM+oil =1000 ml, colour is honey/red.​

Producing methamphetamine hydrochloride.

Start now bubbling this 1000 ml with HCl-gas via 2 L Schlenk flask (or round bottom flask with vacuum quickfit), while this 2 L flask stands in ice bath on magn. mixer and blends vigorously. Check pH frequently, proceed until pH 6. Pour the now acidified 1000 ml in a 2 L evaporation flask and put on Rotavap machine. Spee~100 rpm, t° = 80 °C, little vacuum=0.8 bar (water-jet aspirator is enough), to hold the flask. After distillating off nearly all the DCM, suddenly the contents of the flask turns from dark honey colour to creamy milk color, and it dries out to a round cake on the bottom. Remove the ~0.5 L DCM, now in the collector flask, and hang that empty flask on again. Now put full vacuum on to remove the last traces of water.

Cleaning by 3 x recrystallization: put minimum quantity of hot (40 °C) dry DCM (or dry 98%+ ethanol) in the flask until the last remains of the dry stuff dissolves, and add 4x this DCM-quantity in the form of dry acetone. Close with stopper and put 1 hr in freezer. A solid dirty-white crystal mass is formed with a layer of dark red fluid on top of it. Decant the fluid and repeat this step another 2x and 2 hrs. You have, the last time, snow-white crystals of racemic methamphetamine hydrochloride. Dry Weight = 141.5 g, close to quantitative yield.

Methamphetamine purification.
You can use this technique or follow next advices to produce ICE meth: melt this crystal mass in an alu flat bottom pot on a heater plate at 170-175 °C. Then let this melt, very slowly, and do not go higher than necessary to melt it, or its starts smoking (you have your first quick-test then: enjoy!). Cool down to 150 °C again, really slowly, 1 °C/30 min. (regulate with your temp controller!), and you got ICE, after you let it very slowly again cool down to room temperature (with a closed lid on it!, its hygroscopic!). Advantage: you removed all the water in this process!

You can better make the sulfate salt following logical method: Let 10% H2SO4/Ethanol mix acidifying a 1:4 mix of freebase Meth/Ethanol. This is not so hygroscopic. Filter and dry the crystals.​

G.PattonHello,

After many tests using Methylamine HCL based on this method I will share the best way that I found to obtain Methamphetamine freebase in big scale:

• 966 gr P2P​
• 14 liters Methanol
• 1183 gr Methylamine HCL​
• 638gr NaOH​
• 452 gr Anhydrous Sodium Sulfate​
• 105 gr NaBH4​
• 35 L distilled water​
• 7 Liters DCM​

- Fill the reactor with the 14 L of Methanol
- With stirring dissolve the Methylamine HCL
- Put the reactor temp at 0C(not the mixture temp) and add the NaOH, the temp will increase
- Once the temp come back to 20C add the P2P, the temp will increase stir it during 45min-1 hour
- Add 252gr of anhydrous sodium sulfate
- When the mixture temp arrives to 8C start adding portionwise the NaBH4 not exceeding the 20C
- Once all the NaBH4 has been added let it mixing under 20C during aprox 2 hours until the mixture stops bubbling
- Add the water and continue mixing during 5 min
- Add the DCM and mix it during 10 min
- Stop stirring and let layers get separated
- Keep the bottom layer and discard the upper one( not profitable to extract this aqueous phase)
- Add 200gr of anhydrous sodium sulfate to the saved layer and mix it
- Filter it in Buchner Funnel
- Evaporate the DCM
- Clean and smelly Methamphetamine freebase obtained

;-)

 

[workworkwork]

Hello,

After many tests using Methylamine HCL based on this method I will share the best way that I found to obtain Methamphetamine freebase in big scale:

• 966 gr P2P​
• 14 liters Methanol
• 1183 gr Methylamine HCL​
• 638gr NaOH​
• 452 gr Anhydrous Sodium Sulfate​
• 105 gr NaBH4​
• 35 L distilled water​
• 7 Liters DCM​

- Fill the reactor with the 14 L of Methanol
- With stirring dissolve the Methylamine HCL
- Put the reactor temp at 0C(not the mixture temp) and add the NaOH, the temp will increase
- Once the temp come back to 20C add the P2P, the temp will increase stir it during 45min-1 hour
- Add 252gr of anhydrous sodium sulfate
- When the mixture temp arrives to 8C start adding portionwise the NaBH4 not exceeding the 20C
- Once all the NaBH4 has been added let it mixing under 20C during aprox 2 hours until the mixture stops bubbling
- Add the water and continue mixing during 5 min
- Add the DCM and mix it during 10 min
- Stop stirring and let layers get separated
- Keep the bottom layer and discard the upper one( not profitable to extract this aqueous phase)
- Add 200gr of anhydrous sodium sulfate to the saved layer and mix it
- Filter it in Buchner Funnel
- Evaporate the DCM
- Clean and smelly Methamphetamine freebase obtained

;-)

btcboss2022Can I replace sodium sulfate with magnesium sulfate for the both 2 times it is used?

 

[btcboss2022]

Can I replace sodium sulfate with magnesium sulfate for the both 2 times it is used?

workworkworkYes you can replace it.

 

[G.Patton]

Will the shards be small or will it be a powder?

triwps369Depends on crystallization procedure.

 

[Mr.Blanks00]

Of course is possible I told you I did it, unfortunately I can't share that info my partners don't allow me that because we invest some money to obtain that method. Thanks.

btcboss2022hello btc, after you have separated the isomer from the oil, how many grams of yield do you get from the D isomer and the L isomer whether you throw it away or use it too.

 

[btcboss2022]

hello btc, after you have separated the isomer from the oil, how many grams of yield do you get from the D isomer and the L isomer whether you throw it away or use it too.

Yusuf500gr from L and 300gr from D more or less depend the route to obtain the freebase etc etc

 

[JuanoImano4378]

500gr from L and 300gr from D more or less depend the route to obtain the freebase etc etc

btcboss2022What's the difference between L and D?

 

[johnny.b]

500gr from L and 300gr from D more or less depend the route to obtain the freebase etc etc

btcboss2022How much methylamine I must use to this reaction if I have 33 % solution in methanol

 

[diogenes]

G Pattons initial publication uses freebase, but i think if you were referring to btcboss2022's publication in the comments, he used solid methylamine hcl which he dissolved in methanol. That is my interpretation. Hope this helps

callmecharlieI think btcboss also uses freebase because after adding the Methylamine HCl he add NaOH to the solution, so makes essentially freebase from the HCl salt.

 

[btcboss2022]

I think btcboss also uses freebase because after adding the Methylamine HCl he add NaOH to the solution, so makes essentially freebase from the HCl salt.

diogenesYes Methylamine HCL+NaOH=Methylamine freebase in my case Methylamine HCL is cheaper and I get more freebase amount with less investment.

 

[jotoy]

Yes Methylamine HCL+NaOH=Methylamine freebase in my case Methylamine HCL is cheaper and I get more freebase amount with less investment.

btcboss2022Hi
Im a little confuse. So if i buy methylamine HCL and add it in methanol with sodium hudroxide it will becaome a solution?

 

[hunter12]

So my calculation is right but jusst before using it i need to dry with sulfate?

jotoyYes you use MgSO4, silica gel, 3A molecular sieves or sodium sulfate to dry

 

[jotoy]

Yes you use MgSO4, silica gel, 3A molecular sieves or sodium sulfate to dry

hunter12IVe done that but something weird happen after to much solid stay after reaction and its very thick i e try to do around 33% methylamie solution in methanol

 

[Felix34-73]

I want to pulverize methamphetamine oil and smell like cocaine. How can I do this, can I make a ph 6 and put it in the freezer? should be usable like cocaine

 

[Acab1312]

Hello Does the method of BTCboss2022 use the anhydrous sodium sulafate as a desiccant or are additional desiccants used?

 

[btcboss2022]

Is this just D isomer on its own?

oscar412No, it's separated previously.

 

[btcboss2022]

So have you seperated the isomers and then crystallized the D an L together into that block

oscar412Separate isomers to later cristallize them together dont have any sense you can do that directly from racemic and less work.
The Pic is from D isomer cristallized.

 

[Davidrobinson]

Separate isomers to later cristallize them together dont have any sense you can do that directly from racemic and less work.
The Pic is from D isomer cristallized.

btcboss2022Yer thats what my first question was asking, is that d isomer on its own.

 

[Mr.Blanks00]

can hcl be replaced with isopropyl chloride.

 

[G.Patton]

can hcl be replaced with isopropyl chloride.

Mr.Blanks00no

 

[Charlie3]

Hi guys, if the silica gel is blue in colour. is that okay? or does it have to be transparent?

 

[Hank Schrader]

Chemically speaking, methamphetamine is methamphetamine. No matter what method it is obtained, borohydride or hydrogenation, etc...
But to be honest, NaBH4 methamphetamine is very inferior in terms of time of action and quality.
Perhaps minimal impurities that remain in other production methods and give a specific effect to the product.
In the case of borohydride, the action time is up to 16-18 hours and large dosages of the racemic product.
I think the people who synthesized borohydride methamphetamine would agree with me.
For example, methamphetamine obtained by the leukart method and divided into isomers is effective for almost 2 days.
Received methamphetamine through Sodium borohydride and separated into isomers acts only 16 hours and higher dosage.
The absence of impurities in the base is guaranteed by fractional distillation and division into isomers.
Of course, this sounds very strange, because from a chemical point of view, methamphetamine is methamphetamine, but as practice shows, this is not so.
Using the example of Viagra, I can tell you that fizer is unique in the production of sildenefil, and if you compare it with generics that have a similar amount of active ingredient, you will feel the difference.

 

[mithyl2]

Chemically speaking, methamphetamine is methamphetamine. No matter what method it is obtained, borohydride or hydrogenation, etc...
But to be honest, NaBH4 methamphetamine is very inferior in terms of time of action and quality.
Perhaps minimal impurities that remain in other production methods and give a specific effect to the product.
In the case of borohydride, the action time is up to 16-18 hours and large dosages of the racemic product.
I think the people who synthesized borohydride methamphetamine would agree with me.
For example, methamphetamine obtained by the leukart method and divided into isomers is effective for almost 2 days.
Received methamphetamine through Sodium borohydride and separated into isomers acts only 16 hours and higher dosage.
The absence of impurities in the base is guaranteed by fractional distillation and division into isomers.
Of course, this sounds very strange, because from a chemical point of view, methamphetamine is methamphetamine, but as practice shows, this is not so.
Using the example of Viagra, I can tell you that fizer is unique in the production of sildenefil, and if you compare it with generics that have a similar amount of active ingredient, you will feel the difference.

Hank SchraderWhy is NaBH4 methamphetamine inferior? and is there a way to make it as high quality as other routes of synthesis?

 

[Macondor]

Chemically speaking, methamphetamine is methamphetamine. No matter what method it is obtained, borohydride or hydrogenation, etc...
But to be honest, NaBH4 methamphetamine is very inferior in terms of time of action and quality.
Perhaps minimal impurities that remain in other production methods and give a specific effect to the product.
In the case of borohydride, the action time is up to 16-18 hours and large dosages of the racemic product.
I think the people who synthesized borohydride methamphetamine would agree with me.
For example, methamphetamine obtained by the leukart method and divided into isomers is effective for almost 2 days.
Received methamphetamine through Sodium borohydride and separated into isomers acts only 16 hours and higher dosage.
The absence of impurities in the base is guaranteed by fractional distillation and division into isomers.
Of course, this sounds very strange, because from a chemical point of view, methamphetamine is methamphetamine, but as practice shows, this is not so.
Using the example of Viagra, I can tell you that fizer is unique in the production of sildenefil, and if you compare it with generics that have a similar amount of active ingredient, you will feel the difference.

Hank Schraderand in the MDMA case? can i dm to you?

 

[chuckmcgill]

hello @btcboss2022 @G.Patton I'm following this substituting mdp2p and calculating for molar ratios and something strange happened, instead of dissolving in DCM the organic layer formed a thick sludge like apple sauce in it, making it hard to drain (the sludge tests dark purple/black on marquie reagant like MDMA). We followed your method exactly except we used anhydrous magnesium sulfate instead of your stated dessicant and we used 30% more dessicant than you to make sure it was totally dry. (final Ph of 11 in the water layer)

Do you have any advice for getting the freebase sludge to dissolve into dcm? We cant add dessicant and filter again because the product will stay on the solids

Thanks again cant tell you how much I appreciate your knowledge!

 

[G.Patton]

hello @btcboss2022 @G.Patton I'm following this substituting mdp2p and calculating for molar ratios and something strange happened, instead of dissolving in DCM the organic layer formed a thick sludge like apple sauce in it, making it hard to drain (the sludge tests dark purple/black on marquie reagant like MDMA). We followed your method exactly except we used anhydrous magnesium sulfate instead of your stated dessicant and we used 30% more dessicant than you to make sure it was totally dry. (final Ph of 11 in the water layer)

Do you have any advice for getting the freebase sludge to dissolve into dcm? We cant add dessicant and filter again because the product will stay on the solids

Thanks again cant tell you how much I appreciate your knowledge!

chuckmcgillHi, please, write in appropriate topic. I'll answer there.