(1S,2S,4S,5S)-4,5-Dibromo-2-methyl-cyclohexanecarboxylic acid ((S)-1-phenyl-ethyl)-amide

Base Information

Chemical Name:(1S,2S,4S,5S)-4,5-Dibromo-2-methyl-cyclohexanecarboxylic acid ((S)-1-phenyl-ethyl)-amide
CAS No.:92344-75-7
Molecular Formula:C₁₆H₂₁Br₂NO
Molecular Weight:403.157
Hs Code.:

Synonyms:(1S,2S,4S,5S)-4,5-Dibromo-2-methyl-cyclohexanecarboxylic acid ((S)-1-phenyl-ethyl)-amide

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Chemical Property of (1S,2S,4S,5S)-4,5-Dibromo-2-methyl-cyclohexanecarboxylic acid ((S)-1-phenyl-ethyl)-amide

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Technology Process of (1S,2S,4S,5S)-4,5-Dibromo-2-methyl-cyclohexanecarboxylic acid ((S)-1-phenyl-ethyl)-amide

There total 3 articles about (1S,2S,4S,5S)-4,5-Dibromo-2-methyl-cyclohexanecarboxylic acid ((S)-1-phenyl-ethyl)-amide 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:

: 92344-74-6
(1S,6S)-6-Methyl-cyclohex-3-enecarboxylic acid ((S)-1-phenyl-ethyl)-amide

: 92344-75-7
(1S,2S,4S,5S)-4,5-Dibromo-2-methyl-cyclohexanecarboxylic acid ((S)-1-phenyl-ethyl)-amide

Guidance literature:: With bromine; In dichloromethane; at 0 ℃;
DOI:10.1021/jo00198a012

Reference yield:

: 2627-86-3
(S)-1-phenyl-ethylamine

: 92344-75-7
(1S,2S,4S,5S)-4,5-Dibromo-2-methyl-cyclohexanecarboxylic acid ((S)-1-phenyl-ethyl)-amide

Guidance literature:: Multi-step reaction with 2 steps

1: Et₃N / CH₂Cl₂ / 0 °C

2: Br₂ / CH₂Cl₂ / 0 °C

With bromine; triethylamine; In dichloromethane;
DOI:10.1021/jo00198a012

Reference yield:

: 92284-36-1
(1S,6S)-6-Methyl-cyclohex-3-enecarbonyl chloride

: 92344-75-7
(1S,2S,4S,5S)-4,5-Dibromo-2-methyl-cyclohexanecarboxylic acid ((S)-1-phenyl-ethyl)-amide

Guidance literature:: Multi-step reaction with 2 steps

1: Et₃N / CH₂Cl₂ / 0 °C

2: Br₂ / CH₂Cl₂ / 0 °C

With bromine; triethylamine; In dichloromethane;
DOI:10.1021/jo00198a012