(E)-3-[{4-Chloro-2-[hydroxy-(2,4,6-trimethoxy-phenyl)-methyl]-phenyl}-(2,2-dimethyl-propyl)-carbamoyl]-acrylic acid ethyl ester

Base Information

Chemical Name:(E)-3-[{4-Chloro-2-[hydroxy-(2,4,6-trimethoxy-phenyl)-methyl]-phenyl}-(2,2-dimethyl-propyl)-carbamoyl]-acrylic acid ethyl ester
CAS No.:152909-11-0
Molecular Formula:C₂₇H₃₄ClNO₇
Molecular Weight:520.022
Hs Code.:

Synonyms:(E)-3-[{4-Chloro-2-[hydroxy-(2,4,6-trimethoxy-phenyl)-methyl]-phenyl}-(2,2-dimethyl-propyl)-carbamoyl]-acrylic acid ethyl ester

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Chemical Property of (E)-3-[{4-Chloro-2-[hydroxy-(2,4,6-trimethoxy-phenyl)-methyl]-phenyl}-(2,2-dimethyl-propyl)-carbamoyl]-acrylic acid ethyl ester

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Technology Process of (E)-3-[{4-Chloro-2-[hydroxy-(2,4,6-trimethoxy-phenyl)-methyl]-phenyl}-(2,2-dimethyl-propyl)-carbamoyl]-acrylic acid ethyl ester

There total 5 articles about (E)-3-[{4-Chloro-2-[hydroxy-(2,4,6-trimethoxy-phenyl)-methyl]-phenyl}-(2,2-dimethyl-propyl)-carbamoyl]-acrylic 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: 95.0%

: 26367-48-6
fumaric acid ethyl ester mono chloride

: 152909-10-9
5-chloro-α-(2,4,6-trimethoxyphenyl)-2-(neopentylamino)benzyl alcohol

: 152909-11-0
(E)-3-[{4-Chloro-2-[hydroxy-(2,4,6-trimethoxy-phenyl)-methyl]-phenyl}-(2,2-dimethyl-propyl)-carbamoyl]-acrylic acid ethyl ester

Guidance literature:: With sodium hydrogencarbonate; In dichloromethane; at 20 ℃;
DOI:10.1016/S0968-0896(01)00290-5

Reference yield:

: 621-23-8
1,2,3-trimethoxybenzene

: 152909-11-0
(E)-3-[{4-Chloro-2-[hydroxy-(2,4,6-trimethoxy-phenyl)-methyl]-phenyl}-(2,2-dimethyl-propyl)-carbamoyl]-acrylic acid ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: n-BuLi / tetrahydrofuran; hexane

1.2: 90 percent / tetrahydrofuran; hexane

2.1: 96 percent / NaBH₄ / ethanol

3.1: 72 percent / NaBH₃CN; AcOH / methanol / 20 °C

4.1: 95 percent / NaHCO₃ / CH₂Cl₂ / 20 °C

With sodium tetrahydroborate; n-butyllithium; sodium cyanoborohydride; sodium hydrogencarbonate; acetic acid; In tetrahydrofuran; methanol; ethanol; hexane; dichloromethane;
DOI:10.1016/S0968-0896(01)00290-5

Reference yield:

: 7033-50-3
6-chloro-2-methyl-4H-benzo[d][1,3]oxazin-4-one

: 152909-11-0
(E)-3-[{4-Chloro-2-[hydroxy-(2,4,6-trimethoxy-phenyl)-methyl]-phenyl}-(2,2-dimethyl-propyl)-carbamoyl]-acrylic acid ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: n-BuLi / tetrahydrofuran; hexane

1.2: 90 percent / tetrahydrofuran; hexane

2.1: 96 percent / NaBH₄ / ethanol

3.1: 72 percent / NaBH₃CN; AcOH / methanol / 20 °C

4.1: 95 percent / NaHCO₃ / CH₂Cl₂ / 20 °C

With sodium tetrahydroborate; n-butyllithium; sodium cyanoborohydride; sodium hydrogencarbonate; acetic acid; In tetrahydrofuran; methanol; ethanol; hexane; dichloromethane;
DOI:10.1016/S0968-0896(01)00290-5