Extrakce efedrinu z rostlin

QAZ123123

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1. Ephedrine can be extracted from Ephedra. Cut the stems and branches of Ephedra into 2-4 cm lengths, add 7 times the amount of water, soak and boil 5 times with 0.15MPA hot press for a total of 16 hours to obtain an aqueous solution containing total alkaloids of Ephedra. After the decoction is alkalized to pH 12 with sodium hydroxide, extract it with 2 times the amount of toluene at 60-70°C. Add 2% oxalic acid solution to the toluene extract to make the pH of the toluene layer 7, transfer the total alkaloids in the toluene extract to the oxalic acid solution, separate the toluene layer, and obtain a dilute oxalate solution of total alkaloids of Ephedra. Concentrate the dilute oxalic acid solution containing alkaloids at 70°C under reduced pressure and cool to 30°C. The solubility of ephedrine oxalate in water is relatively low, and the mother liquor contains pseudoephedrine oxalate.
2. Add 8-10 times water and 1.5% activated carbon, boil, filter, and add calcium chloride solution to the filtrate under stirring until no precipitation or turbidity occurs to obtain ephedrine hydrochloride solution. Then add sodium sulfide solution to pH 7.5-8, and precipitate impurities such as calcium oxalate and iron sulfide. After filtering, take the supernatant and add hydrochloric acid to adjust the pH to 6-6.5, filter, reduce the pressure and concentrate the solution, cool to 30°C, crystallize, centrifuge, and dry to obtain the finished product.
3. Alkalize the mother liquor containing pseudoephedrine oxalate with sodium hydroxide to separate pseudoephedrine, and then acylate, transfer, hydrolyze, and neutralize to obtain ephedrine oxalate crystals, and then treat as above to obtain ephedrine hydrochloride.
Is this method okay?
 

Eleusius_hive_reboot

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To Complete this Discussion ...
::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::
i'll provide my IN-DEPTH LAB-JOURNALS,
Everything,
regarding EPHEDRA as source Material.
~~~~~~~~~~~ ~~~~~~~~~~~~~~~~ ~~~~~~~~~~~~~~~~
👇😸👍

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VdrhuXLPqR SQgO4wqrHb DyEt6jBgSC KJ3DeNskQH 7YIc9kKHjo AWf1iYwGjT QefpXIual8 F3GBwKNqJO D6qYZykVXs ToNQTSYAWe
 
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Thanks , can i go this route? 80% METHANOL extration then dilute it with water to 40w/w then add ammonia then do liquid - liquid extraction. Then evaporate dcm and dissolve in tolune then introduce HCL gas . Is this gonna work? How much lower purity and yield iam gonna get?
 
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It cant be turned into D_ methamphetamine right becaus ephedera sinica contains L_ephederine? Pls answer
 

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Hi, you can get racemic meth and then separate isomers.
 
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Thanks for your response . Its not gonna be 50/50 ? Because most of the ephedera sisnica is L_ephederine and L_ ephederine always is reduced to L_meth am i right?
 

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Its up to synthesis way. It can be not 50/50 exactly.
 
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I will use iodine phosphorous method, could you give me a estimation that how much will be D methamphetamine? Appriciate it.
 

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I can't answer, something around. 30/70, 70/30, 40/60 and so one.
 

Arakava

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Can't we use tartaric acid on extracted ephedrine to seperate isomers and obtain D isomer first then use D-ephedrine in synthesis?
 
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I found ephedera but its ephederine concentration is not specified , what is the least amount that it can contain do i have to get over 2kg for 6g of ephederine?
 

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Nice science article!!!!

For a pound of dried ephedra, could get at least 7 grams of ephedrine alkaloids
 

Eleusius_hive_reboot

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i'll assure that the ACETIC method is the way to go....(IN ALMOST A YEAR of constant stash grilling, i never bought a box again once (of pseudo i mean...)

finest Meth outcome....!

The ephedra pre-treatment counts!
just dry it hard
, grind it until you go CRAZY.
and then soak that bitch up as described

[ i have always some big ass jugs on spare at once]

Every few moments i:
-------------------------

  1. crudely filter the brew loosely with a common linen-shoppingbag...squeeze---->
  2. BASE(NAOH + excess NaCl)----->

  3. Collect Petroleum/VM&P-naphta hydrocarbon mixture with E-BASE---->

  4. NP-Layer+100mls DH2O & HCLaq.

  5. until 5-6~PH and - magstir it ----->


  6. seperate non-polar and save for next run---->

  7. Acid/Water solution smashed in to Fat pyrex Beaker

  8. with a heavy venting-Fan over surface and vape with sufficient heat until skin forms......

  9. ACETONE dashings + rinse + r-xtallize with IPA-----BOOM
 
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