No video, but I can advise in detail on the process here, private message or XMPP. I have enough practical experience on this synthesis.
JWH-018 synthesis
No, time does not decrease. We cannot use nitromethane, we get a product, but the yield will be lowered, and it will be more difficult to clean. Maybe you can buy 1,1,1,3,3,3-hexafluoroisopropanol (HFIP)? Although its price does not allow being the best option.
Last edited by a moderator:
- By aa1178251182
Sir, can HFIP replace nitromethane?
Does anyone have access to this noid ?
- By Marc-BenzoScam
That's the million dollar question Frenchie. I guess I'm below a noob because I'm definitely not a chemist but I can move some shit.
Hi, we ordered the 109555-87-5 direct from supplier, but they sent 83-34-1.....3-methylindole.
Could this product replace the 109555-87-5 in this synthesis?
If not is there another route using the 83-34-1 or is this product no good.
Help appriechated.
Could this product replace the 109555-87-5 in this synthesis?
If not is there another route using the 83-34-1 or is this product no good.
Help appriechated.
- By HerrHaber
Sorry mate the suppliers seem to be mocking you 3-methyl indole is also known as skatole and it is the litteral smell of shit (I'm afraid I'm not joking) and unfortunately it can't be used for the preparation because the 3 position is occupied by methyl (did not say it is impossible since oxidation of the methyl to carboxylic acid which in turn could theoretically rather than in practice be converted to the acyl chloride to further Friedel-Crafts it with naphtalene is just my imagination and never heard of anyone doing this) Best advice is buy indole since it's probably the cheapest building block in the whole molecule.
hi friends, i want ask, the ones with success in JWH-018 synthesis:
is anyone located in europe and able, to sell maybe a small amount or more of the finished product?
pm please
is anyone located in europe and able, to sell maybe a small amount or more of the finished product?
pm please
Please help about Tin (IV) chloride, I could not get it, and I found Tin (Il) chloride in a solid state, not a liquid, so can I use it in the reaction
- By HerrHaber
SnCl2 (stannous chloride) is not a strong Lwis acid that is needed to catalize the acylation reaction; you can find a preparation on youtube where the target compound is tin triblutyl hydride but SnCl4 is prepared as an intermediate from Sn metal powder in a heated tube thru which Cl2 is passed. This is hardcore chemistry so it shouldn't be attempted by amateurs not that jwh018 is
In the second and final step, I fixed the temperature at 70 degrees Celsius, and in the end the product came out weak. Accordingly, what is the temperature required for the reaction in the last stage?
In the first step, I succeeded in obtaining it in solid form. And I tried to recrystallize it with ethanol, but it didn't get well, so I recrystallized it with IPA. And the second step is the reaction I tried to recrystalization with ipa without solidifying it properly because I was in a hurry. But it was not obtained in a solid state. Do I have to do something solid when recrystallizing? And what is the most suitable recrystallization solvent in step 2?