4-[2-(3-bromo-phenyl)-2-(4'-chloro-2'-methylbiphenyl-4-ylcarbamoyl)ethyl]benzoic acid tert-butyl ester

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Chemical Name:4-[2-(3-bromo-phenyl)-2-(4'-chloro-2'-methylbiphenyl-4-ylcarbamoyl)ethyl]benzoic acid tert-butyl ester
CAS No.:1207989-36-3
Molecular Formula:C₃₃H₃₁BrClNO₃
Molecular Weight:604.971
Hs Code.:

Synonyms:4-[2-(3-bromo-phenyl)-2-(4'-chloro-2'-methylbiphenyl-4-ylcarbamoyl)ethyl]benzoic acid tert-butyl ester

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Chemical Property of 4-[2-(3-bromo-phenyl)-2-(4'-chloro-2'-methylbiphenyl-4-ylcarbamoyl)ethyl]benzoic acid tert-butyl ester

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Technology Process of 4-[2-(3-bromo-phenyl)-2-(4'-chloro-2'-methylbiphenyl-4-ylcarbamoyl)ethyl]benzoic acid tert-butyl ester

There total 6 articles about 4-[2-(3-bromo-phenyl)-2-(4'-chloro-2'-methylbiphenyl-4-ylcarbamoyl)ethyl]benzoic acid tert-butyl ester 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: 88.0%

: 1207989-35-2
4′-chloro-2′-methylbiphenyl-4-amine

: 1207989-34-1
4-[2-carboxy-2-(3-bromophenyl)ethyl]benzoic acid tert-butyl ester

: 1207989-36-3
4-[2-(3-bromo-phenyl)-2-(4'-chloro-2'-methylbiphenyl-4-ylcarbamoyl)ethyl]benzoic acid tert-butyl ester

Guidance literature:: 4-[2-carboxy-2-(3-bromophenyl)ethyl]benzoic acid tert-butyl ester; With oxalyl dichloride; In dichloromethane; at 20 ℃; for 14h;

4′-chloro-2′-methylbiphenyl-4-amine; With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 - 20 ℃; for 14h;

Reference yield:

: 1207989-32-9
(R)-4-benzyl-3-(2-(3-bromophenyl)acetyl)oxazolidin-2-one

: 1207989-36-3
4-[2-(3-bromo-phenyl)-2-(4'-chloro-2'-methylbiphenyl-4-ylcarbamoyl)ethyl]benzoic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: lithium hexamethyldisilazane / tetrahydrofuran / 1.5 h / -78 °C

1.2: 2 h / -78 °C

2.1: lithium hydroxide; dihydrogen peroxide / tetrahydrofuran; water / 3 h / 20 °C

3.1: oxalyl dichloride / dichloromethane / 14 h / 20 °C

3.2: 14 h / 0 - 20 °C

With oxalyl dichloride; dihydrogen peroxide; lithium hydroxide; lithium hexamethyldisilazane; In tetrahydrofuran; dichloromethane; water;

Reference yield:

: 1207989-33-0
4-{3-(4-benzyl-2-oxooxazolidin-3-yl)-2-(3-bromophenyl)-3-oxopropyl}benzoic acid tert-butyl ester

: 1207989-36-3
4-[2-(3-bromo-phenyl)-2-(4'-chloro-2'-methylbiphenyl-4-ylcarbamoyl)ethyl]benzoic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: lithium hydroxide; dihydrogen peroxide / tetrahydrofuran; water / 3 h / 20 °C

2.1: oxalyl dichloride / dichloromethane / 14 h / 20 °C

2.2: 14 h / 0 - 20 °C

With oxalyl dichloride; dihydrogen peroxide; lithium hydroxide; In tetrahydrofuran; dichloromethane; water;