(8-bromo-4-methyl-1,2,3,4-tetrahydro-cyclopenta[b]indol-5-yl)-phenyl-methanol

Base Information

Chemical Name:(8-bromo-4-methyl-1,2,3,4-tetrahydro-cyclopenta[b]indol-5-yl)-phenyl-methanol
CAS No.:604788-58-1
Molecular Formula:C₁₉H₁₈BrNO
Molecular Weight:356.262
Hs Code.:

(8-bromo-4-methyl-1,2,3,4-tetrahydro-cyclopenta[<i>b</i>]indol-5-yl)-phenyl-methanol

Synonyms:(8-bromo-4-methyl-1,2,3,4-tetrahydro-cyclopenta[b]indol-5-yl)-phenyl-methanol

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (8-bromo-4-methyl-1,2,3,4-tetrahydro-cyclopenta[b]indol-5-yl)-phenyl-methanol

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Technology Process of (8-bromo-4-methyl-1,2,3,4-tetrahydro-cyclopenta[b]indol-5-yl)-phenyl-methanol

There total 3 articles about (8-bromo-4-methyl-1,2,3,4-tetrahydro-cyclopenta[b]indol-5-yl)-phenyl-methanol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 85.0%

: 100-52-7
benzaldehyde

: 604788-30-9
5,8-dibromo-4-methyl-1,2,3,4-tetrahydro-cyclopenta[b]indole

: 604788-58-1
(8-bromo-4-methyl-1,2,3,4-tetrahydro-cyclopenta[b]indol-5-yl)-phenyl-methanol

Guidance literature:: 5,8-dibromo-4-methyl-1,2,3,4-tetrahydro-cyclopenta[b]indole; With tert.-butyl lithium; In diethyl ether; at -78 ℃; for 0.25h;

benzaldehyde; In diethyl ether;
DOI:10.1016/S0040-4039(03)01482-5

Reference yield:

: 62672-26-8
(2,5-dibromophenyl)hydrazine

: 604788-58-1
(8-bromo-4-methyl-1,2,3,4-tetrahydro-cyclopenta[b]indol-5-yl)-phenyl-methanol

Guidance literature:: Multi-step reaction with 3 steps

1.1: 83 percent / BF₃*acetic acid complex / acetic acid / 1 h

2.1: t-BuLi / diethyl ether / 0.25 h / -78 °C

2.2: 85 percent / diethyl ether

With tert.-butyl lithium; borontrifluoride acetic acid; In diethyl ether; acetic acid; 1.1: Fisher indole reaction;
DOI:10.1016/S0040-4039(03)01482-5

Reference yield:

: 120-92-3
cyclopentanone

: 604788-58-1
(8-bromo-4-methyl-1,2,3,4-tetrahydro-cyclopenta[b]indol-5-yl)-phenyl-methanol

Guidance literature:: Multi-step reaction with 3 steps

1.1: 83 percent / BF₃*acetic acid complex / acetic acid / 1 h

2.1: t-BuLi / diethyl ether / 0.25 h / -78 °C

2.2: 85 percent / diethyl ether

With tert.-butyl lithium; borontrifluoride acetic acid; In diethyl ether; acetic acid; 1.1: Fisher indole reaction;
DOI:10.1016/S0040-4039(03)01482-5