9-methyl-3-(p-toluenesulfonyl)-1-vinyl-2,3,4,5-tetrahydro-1H-benzo[d]azepine

Base Information

Chemical Name:9-methyl-3-(p-toluenesulfonyl)-1-vinyl-2,3,4,5-tetrahydro-1H-benzo[d]azepine
CAS No.:1428536-65-5
Molecular Formula:C₂₀H₂₃NO₂S
Molecular Weight:341.474
Hs Code.:

Synonyms:9-methyl-3-(p-toluenesulfonyl)-1-vinyl-2,3,4,5-tetrahydro-1H-benzo[d]azepine

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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 9-methyl-3-(p-toluenesulfonyl)-1-vinyl-2,3,4,5-tetrahydro-1H-benzo[d]azepine

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Technology Process of 9-methyl-3-(p-toluenesulfonyl)-1-vinyl-2,3,4,5-tetrahydro-1H-benzo[d]azepine

There total 2 articles about 9-methyl-3-(p-toluenesulfonyl)-1-vinyl-2,3,4,5-tetrahydro-1H-benzo[d]azepine 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:

: trans-N-(4-bromobut-2-enyl)-N-(3-methylphenethyl)-p-toluenesulfonamide

: 1428536-64-4
7-methyl-3-(p-toluenesulfonyl)-1-vinyl-2,3,4,5-tetrahydro-1H-benzo[d]azepine

: 1428536-65-5
9-methyl-3-(p-toluenesulfonyl)-1-vinyl-2,3,4,5-tetrahydro-1H-benzo[d]azepine

Guidance literature:: With bismuth(lll) trifluoromethanesulfonate; In dichloromethane; at 20 ℃; for 16h; Overall yield = 78 %; regioselective reaction; Molecular sieve; Inert atmosphere;
DOI:10.1016/j.tetlet.2013.02.012

Reference yield:

: 245469-20-9
4-methyl-N-(2-m-tolyl-ethyl)-benzenesulfonamide

: 1428536-64-4
7-methyl-3-(p-toluenesulfonyl)-1-vinyl-2,3,4,5-tetrahydro-1H-benzo[d]azepine

: 1428536-65-5
9-methyl-3-(p-toluenesulfonyl)-1-vinyl-2,3,4,5-tetrahydro-1H-benzo[d]azepine

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / N,N-dimethyl-formamide / 20 °C / Inert atmosphere

2: bismuth(lll) trifluoromethanesulfonate / dichloromethane / 16 h / 20 °C / Molecular sieve; Inert atmosphere

With bismuth(lll) trifluoromethanesulfonate; potassium carbonate; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.tetlet.2013.02.012