video synthesis

Stage one: 1-Phenylpropan-1-one Bromination Stage two: Preparation and Washing of Methcathinone Hydrochloride Stage three: Methcathinone Hydrochloride Formation Edit: 6:20 - 125 ml of ethyl acetate https://bbgate.com/threads/synthesis-of-methcathinone-hydrochloride-from-propiophenone.9410

Synthesis of JWH-018 from 3-(1-Naphthoyl)indole. 3-(1-Naphthoyl)indole synthesis from indole. https://bbgate.com/threads/jwh-018-synthesis-video.9134/

Introduction BB Forum team glad to represent elementary and simple ADB-PINACA synthesis, which is not require rare or elaborated equipment. There is step-by-step video guide and clear write up about ADB-PINACA formation with a good yield. This synthesis can be repeated even by chemistry...

Video of ADB-PINACA Preparation from methyl 1H-indazole-3-carboxylate https://bbgate.com/threads/adb-pinaca-synthesis-video.8750/

Introduction This synthesis is a good option in case you have unavailable phenylacetone for further amphetamine or methamphetamine synthesis. BMK glycidate can be easily turn into P2P by hydrolysis. This reaction have some pros and cons. The main disadvantage that reaction is very sensitive to...

The yield is 79%* https://bbgate.com/threads/bmk-glycidate-sodium-salt-synthesis-from-benzaldehyde.6134/

Phenylacetone (P2P) synthesis from P2NP. https://bbgate.com/threads/p2p-synthesis-from-p2np.188/

Amphetamine synthesis via NaBH4 reductive amination from P2NP. https://bbgate.com/threads/one-pot-amphetamine-synthesis-from-p2np-with-nabh4-cucl2-1kg-scale.70/

479Mb (.mp4) 1-Phenyl-2-nitropropene (P2NP) reduction to α-methylphenylethylamine by aluminium amalgam. https://bbgate.com/threads/amphetamine-synthesis-from-p2np-via-al-hg-video.196/

✅This method is suitable for the synthesis of Mescaline and its analogues (look Pihkal). ☣️Exhaust ventilation, respiratory and eye protection are needed.

https://bbgate.com/threads/synthesis-of-amphetamine-from-p2np-via-al-hg-video.196/

Methyl 1H-Indazole-3-carboxylate 1. A solution of indazole-3-carboxylic acid (100 g) in MeOH (1500 ml) was treated with conc. H2SO4 (100 ml). 2. Heated at reflux for 4 h. 3. The mixture was concentrated in vacuo and dissolved in EtOAc (2500 ml). 4. The organic phase was washed with sat. aq...