5'-(4-ethoxycarbonylmethoxy-2,6-dimethylbenzyl)-3'-isopropyl-2'-methoxymethoxybiphenyl-4-carboxylic acid

Base Information

Chemical Name:5'-(4-ethoxycarbonylmethoxy-2,6-dimethylbenzyl)-3'-isopropyl-2'-methoxymethoxybiphenyl-4-carboxylic acid
CAS No.:417871-88-6
Molecular Formula:C₃₁H₃₆O₇
Molecular Weight:520.623
Hs Code.:

Synonyms:5'-(4-ethoxycarbonylmethoxy-2,6-dimethylbenzyl)-3'-isopropyl-2'-methoxymethoxybiphenyl-4-carboxylic acid

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Chemical Property of 5'-(4-ethoxycarbonylmethoxy-2,6-dimethylbenzyl)-3'-isopropyl-2'-methoxymethoxybiphenyl-4-carboxylic acid

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Technology Process of 5'-(4-ethoxycarbonylmethoxy-2,6-dimethylbenzyl)-3'-isopropyl-2'-methoxymethoxybiphenyl-4-carboxylic acid

There total 4 articles about 5'-(4-ethoxycarbonylmethoxy-2,6-dimethylbenzyl)-3'-isopropyl-2'-methoxymethoxybiphenyl-4-carboxylic acid 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: 89.0%

: 105-36-2
ethyl bromoacetate

: 417871-64-8
5'-(4-hydroxy-2,6-dimethylbenzyl)-3'-isopropyl-2'-methoxymethoxybiphenyl-4-carboxylic acid

: 417871-88-6
5'-(4-ethoxycarbonylmethoxy-2,6-dimethylbenzyl)-3'-isopropyl-2'-methoxymethoxybiphenyl-4-carboxylic acid

Guidance literature:: With caesium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 0.5h;
DOI:10.1016/S0968-0896(01)00284-X

Reference yield:

: 328236-46-0
3,5-dimethyl-4-(3'-isopropyl-4'-O-methoxymethylbenzyl)-O-triisopropylsilylphenol

: 417871-88-6
5'-(4-ethoxycarbonylmethoxy-2,6-dimethylbenzyl)-3'-isopropyl-2'-methoxymethoxybiphenyl-4-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: n-BuLi / tetrahydrofuran; hexane / 2 h / 20 °C

1.2: tetrahydrofuran; hexane / 1 h / 20 °C

2.1: 71 percent / Pd₂(dba)3*CHCl₃; Cs₂CO₃ / toluene; ethanol / 8 h / Heating

3.1: 90 percent / Bu₄NF / tetrahydrofuran

4.1: 89 percent / Cs₂CO₃ / dimethylformamide / 0.5 h / 20 °C

With tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; n-butyllithium; tetrabutyl ammonium fluoride; caesium carbonate; In tetrahydrofuran; ethanol; hexane; N,N-dimethyl-formamide; toluene; 2.1: Suzuki coupling;
DOI:10.1016/S0968-0896(01)00284-X

Reference yield:

: 417871-20-6
{5'-[2,6-dimethyl-4-(triisopropylsilanyloxy)benzyl]-3-isopropyl-2-methoxymethoxyphenyl}boronic acid

: 417871-88-6
5'-(4-ethoxycarbonylmethoxy-2,6-dimethylbenzyl)-3'-isopropyl-2'-methoxymethoxybiphenyl-4-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 71 percent / Pd₂(dba)3*CHCl₃; Cs₂CO₃ / toluene; ethanol / 8 h / Heating

2: 90 percent / Bu₄NF / tetrahydrofuran

3: 89 percent / Cs₂CO₃ / dimethylformamide / 0.5 h / 20 °C

With tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; tetrabutyl ammonium fluoride; caesium carbonate; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide; toluene; 1: Suzuki coupling;
DOI:10.1016/S0968-0896(01)00284-X