6-allyl-5-allyloxy-4-(allyl-phenyl-amino)-4'-chloro-3-methyl-biphenyl-2-carboxylic acid ethyl ester

Base Information

Chemical Name:6-allyl-5-allyloxy-4-(allyl-phenyl-amino)-4'-chloro-3-methyl-biphenyl-2-carboxylic acid ethyl ester
CAS No.:1190367-08-8
Molecular Formula:C₃₁H₃₂ClNO₃
Molecular Weight:502.053
Hs Code.:

Synonyms:6-allyl-5-allyloxy-4-(allyl-phenyl-amino)-4'-chloro-3-methyl-biphenyl-2-carboxylic acid ethyl ester

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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 6-allyl-5-allyloxy-4-(allyl-phenyl-amino)-4'-chloro-3-methyl-biphenyl-2-carboxylic acid ethyl ester

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Technology Process of 6-allyl-5-allyloxy-4-(allyl-phenyl-amino)-4'-chloro-3-methyl-biphenyl-2-carboxylic acid ethyl ester

There total 1 articles about 6-allyl-5-allyloxy-4-(allyl-phenyl-amino)-4'-chloro-3-methyl-biphenyl-2-carboxylic acid ethyl 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:

: C₂₅H₂₄ClNO₃

: 106-95-6
allyl bromide

: 1190367-08-8
6-allyl-5-allyloxy-4-(allyl-phenyl-amino)-4'-chloro-3-methyl-biphenyl-2-carboxylic acid ethyl ester

Guidance literature:: With sodium hydride; In N,N-dimethyl-formamide;
DOI:10.1039/b910397j

Reference yield: 40.0%

: 1190367-08-8
6-allyl-5-allyloxy-4-(allyl-phenyl-amino)-4'-chloro-3-methyl-biphenyl-2-carboxylic acid ethyl ester

: 1190367-25-9
9-(allyl-phenyl-amino)-6-(4-chloro-phenyl)-8-methyl-2,5-dihydro-benzo[b]oxepine-7-carboxylic acid ethyl ester

: 1190367-24-8
10-allyl-9-(4-chloro-phenyl)-7-methyl-6-phenyl-5,6-dihydro-2H-benzo[b][1,4]oxazocine-8-carboxylic acid ethyl ester

Guidance literature:: With Grubbs catalyst first generation; In dichloromethane; at 25 ℃; regioselective reaction; Inert atmosphere;
DOI:10.1039/b910397j