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Hello Breaking Bad!
We present to your attention the long-awaited material on the synthesis of the most famous and best synthetic cannabinoid!
The synthesis is very simple from completely legal reagents.
It is also worth noting that you can work in several directions:
- synthesis and sale of semi-finished product (3-(1-Naphthoyl)indole)
- synthesis and sale of JWH-018
- production of smoking blends

In the near future, a video clip will be released on the production of synthetic hashish based on JWH-018, obtained during this work.
 
i now. I meant that the indole nitrogen reacts with the acidic proton. like hcl and...
Oh, right. I have confused myself, sorry. Sounds correct but I never heard about salt form. Probably steric hurdles prevent this formation. Cl atom is quite large.
 
Hello Breaking Bad!
We present to your attention the long-awaited material on the synthesis of the most famous and best synthetic cannabinoid!
The synthesis is very simple from completely legal reagents.
It is also worth noting that you can work in several directions:
- synthesis and sale of semi-finished product (3-(1-Naphthoyl)indole)
- synthesis and sale of JWH-018
- production of smoking blends

In the near future, a video clip will be released on the production of synthetic hashish based on JWH-018, obtained during this work.
We hope to see a video of cannabis manufacturing soon. I truly thank you for your efforts
 
Oh, right. I have confused myself, sorry. Sounds correct but I never heard about salt form. Probably steric hurdles prevent this formation. Cl atom is quite large.
It is an interesting topic. If you are a manufacturer, I suggest you do this test and make its salt.

It was a good video.
 
Hello,
I have a question regarding this synthesis. Why is N1 alkylation of indole performed as a last step. Can we acylate N-alkyl indole in the same C3 manner with specificity?
Thank you,
WoodChipperr.
 
would this be an option if you have low quality plant material but wish to make it more profitable? or is it very must distinguishable from a cannabis high?
 
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Hi , thank you for the video , just a question what is the HPLC purity % ? (on the video above) ,what do you guys think about this patent purification/recristalization method ?: ! CN102838525A !
1-pentyl-3-(1 naphthoyl) indole bullion
drop into above-mentioned thick wet article in the 120ml methyl alcohol, and temperature rising reflux 1h is cooled to 15 ± 1 ℃, and filtration is watered with cold methanol and to be washed, drain refining wet article 56g; To make with extra care wet article and drop into vacuum rotary furnace drying bipyramid, be evacuated to-0.09Mpa, the logical circulating hot water oven dry of chuck; Water temperature is controlled at 55~60 ℃ of oven dry 7.5h, after offgas duct turns cold, is cooled to 25 ℃ of dischargings; Get 1-pentyl-3-(1 naphthoyl) indole product 51.5g; Yield 94.0%, purity (HPLC): 99.0%, M.P:66.5~67.4 ℃.
 
would this be an option if you have low quality plant material but wish to make it more profitable? or is it very must distinguishable from a cannabis high?
Hello,
are you referring to combining a low quality canabis plant with JWH-018 and selling it for more and if the high can be distinguishable ?
 
Well yes, I realize it isn't ethical, and I'm not exactly he'll set on doing it but it's just a hypothetical question. I don't see the harm. In asking tho I understand you don't want to be accosciated with emergency room trips if someone does this. Actually I'm interested in both and if the high is the same would it be detectable in thc urine test?
 
Well yes, I realize it isn't ethical, and I'm not exactly he'll set on doing it but it's just a hypothetical question. I don't see the harm. In asking tho I understand you don't want to be accosciated with emergency room trips if someone does this. Actually I'm interested in both and if the high is the same would it be detectable in thc urine test?
The high is slightly different although depends on the quantity. Synthetic cannabinoids are way more potent then the plant. I'm pretty sure that yes synthetic cannabinoids are detectable in THC tests because synthetic cannabinoids trigger THC receptors in the brain with release the same metabolites as canabis although this is not applicable by all synthetic cannabinoids. My personal opinion is that drugs should not be associated with money and they should be widely available, so as in for the potential profits out of selling low quality weed laced with synthetic cannabinoids (although unethical) I really don't know.
-WC
 
Last edited:
I have a question regarding this synthesis. Why is N1 alkylation of indole performed as a last step. Can we acylate N-alkyl indole in the same C3 manner with specificity?
Sorry, can you formulate your question clearly. About what specificity are you talking about?
 
Hi, I don't have access to indole and naphthoyl, their cost is more expensive than hashish itself. Can you post a video of their synthesis?
 
hello

Can someone give me the contact information of a supplier that has all the necessary ingredients to cook the recipe?

I have contacted some suppliers but they don't answer...
 
I have tried this synthesis exactly like the video, there is no cannabinoid effect ! waste of money !
 
AHas anyone here tried it and succeeded in making Jwh 018? If so, please contact me, I will give you money via BTC.
 
Sorry if this isn't the right place to post.
A while ago I tried this synthesis by changing a few reagents:
AlCl3 was replaced by ZnCl2.
TBAB was replaced by DDAC (Didecyldimethylammonium chloride), a phase catalyst found OTC in disinfectants and anti-algae products.

With these changes, the 3-(1-naphthoyl)indole didn't precipitate, and I had to evaporate the DCM for it to precipitate. The 3-(1-naphthoyl)indole obtained was pink/red and my attempts to purify it by recrystallization were unsuccessful. One of the forum experts advised me to make a solution with 10% NaOH in 50:50 water:ethanol for recrystallization, which seemed to work, giving me a beige/white product.
So I moved on to the next stage, using the somewhat impure 3-(1-naphthoyl)indole, but replacing the TBAB with DDAC. The DDAC was obtained by evaporating most of the water found in an anti-algae product containing almost exclusively DDAC. This concentrated aqueous solution of DDAC replaced the TBAB. I might add that this solution contained a small amount of pink dye, which didn't seem to pose any problems for the reaction.
In the end, a yellow product was obtained, which was left in the open air for a few weeks, as a smell of 1-bromopentane could still be detected.

After a few weeks, the smell had disappeared and the product was dark orange, some of the oil having partially crystallized. The melting point corresponded perfectly to JWH-018. Out of curiosity, I even made a Liebermann reagent, which on contact with the substance turned brown, a color that correspond to JWH-018.
(https://en.wikipedia.org/wiki/Liebermann_reagent)
 
Hola, en Alibaba me venden cloruro de 1-naftoilo pero en forma líquida. Si lo compro líquido ¿cuánto etanol debo diluir?
 
Sorry, can you formulate your question clearly. About what specificity are you talking about?
i used benzoyl chloride i tried to make a simpler version the same reaction and it was strange sometimes strong can make you black out sometimes weak what's the problem
 
Reflux for how long exactly? (The video doesn't specify)
Hello, there is no exact time. You need to control the reaction and finish reflux after until the boiling is slowing down. It's noticeable, the bubbles become smaller, the mixture thickens. Approximate range is ~15-40 min.
 
i
Hello Breaking Bad!
We present to your attention the long-awaited material on the synthesis of the most famous and best synthetic cannabinoid!
The synthesis is very simple from completely legal reagents.
It is also worth noting that you can work in several directions:
- synthesis and sale of semi-finished product (3-(1-Naphthoyl)indole)
- synthesis and sale of JWH-018
- production of smoking blends

In the near future, a video clip will be released on the production of synthetic hashish based on JWH-018, obtained during this work.
am from a third world country we dont have 1 Naphtoyl Chloride at all we dont even have DMC we have Methyline Chloride , i can only get Naphthalene balls and Aluminim Chloride and Indole , what should i do please advice
 
i

am from a third world country we dont have 1 Naphtoyl Chloride at all we dont even have DMC we have Methyline Chloride , i can only get Naphthalene balls and Aluminim Chloride and Indole , what should i do please advice
You can synthesize 3-(1-Naphthoyl)indole and 1-naphthoyl chloride by yourself.

P.S. Don't post same messages please to avoid ban for spam.
 
First of all, hats off to the author
Seeing that some people were skeptical about the final result before, I tested it myself and it definitely works!
But also encountered problems do not know how to solve?
1, the final oil has been in the sun for 3 days and still has the 1-bromopentane smell, I put it on cigarettes and the smell is devastating, looking for a solution!
2, the oily substance and the e-cigarette oil will still be layered after mixing, how can I blend the e-cigarette oil perfectly?
These two issues are bothering me and I'm hoping someone who knows can give me some advice! Thanks a lot!
 

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