## Abstract The Batcho–Leimgruber strategy was employed to synthesize 3‐(2‐dimethylamino‐[^2^H~4~]‐ethyl)‐1__H__‐indol‐5‐ol (bufotenine, 5‐HO‐DMT) (**8**) from commercial 3‐methyl‐4‐nitro‐phenol (**1**), benzyl bromide and __N,N__–dimethylformamide–dimethylacetal. Compound **4** was synthesized fro
Synthesis of deuterium labeled standards of 5-methoxy-N,N-dimethyltryptamine (5-Meo-DMT)
✍ Scribed by Ya-Zhu Xu; Chinpiao Chen
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- French
- Weight
- 108 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
The Batcho-Leimgruber strategy was employed to synthesize 5-[ 2 H 3 ]-methoxy-1 H-indole 4 from commercially available 5-hydroxy-2-nitrotoluene 1 and CD 3 I. Compound 4 was treated with oxalyl chloride, dimethylamine and lithium aluminum hydride to yield 5-[ 2 H 3 ]-methoxy-N,N-dimethyltryptamine 6.
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