2-oxo-5-[4-(4-phenyl-5-trifluoromethyl-thiophen-2-ylmethoxy)-phenyl]-pyrrolidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl ester

Base Information

Chemical Name:2-oxo-5-[4-(4-phenyl-5-trifluoromethyl-thiophen-2-ylmethoxy)-phenyl]-pyrrolidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl ester
CAS No.:899808-30-1
Molecular Formula:C₃₀H₃₀F₃NO₆S
Molecular Weight:589.633
Hs Code.:

2-oxo-5-[4-(4-phenyl-5-trifluoromethyl-thiophen-2-ylmethoxy)-phenyl]-pyrrolidine-1,3-dicarboxylic acid 1-<i>tert</i>-butyl ester 3-ethyl ester

Synonyms:2-oxo-5-[4-(4-phenyl-5-trifluoromethyl-thiophen-2-ylmethoxy)-phenyl]-pyrrolidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl ester

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Chemical Property of 2-oxo-5-[4-(4-phenyl-5-trifluoromethyl-thiophen-2-ylmethoxy)-phenyl]-pyrrolidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl ester

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Technology Process of 2-oxo-5-[4-(4-phenyl-5-trifluoromethyl-thiophen-2-ylmethoxy)-phenyl]-pyrrolidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl ester

There total 7 articles about 2-oxo-5-[4-(4-phenyl-5-trifluoromethyl-thiophen-2-ylmethoxy)-phenyl]-pyrrolidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-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: 83.0%

: 899808-29-8
2-oxo-5-[4-(4-phenyl-5-trifluoromethyl-thiophen-2-ylmethoxy)-phenyl]-pyrrolidine-1-carboxylic acid tert-butyl ester

: 541-41-3
chloroformic acid ethyl ester

: 899808-30-1
2-oxo-5-[4-(4-phenyl-5-trifluoromethyl-thiophen-2-ylmethoxy)-phenyl]-pyrrolidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl ester

Guidance literature:: 2-oxo-5-[4-(4-phenyl-5-trifluoromethyl-thiophen-2-ylmethoxy)-phenyl]-pyrrolidine-1-carboxylic acid tert-butyl ester; With lithium hexamethyldisilazane; In tetrahydrofuran; at -78 ℃;

chloroformic acid ethyl ester; In tetrahydrofuran; at -78 ℃;
DOI:10.1016/j.bmcl.2006.03.090

Reference yield:

: 899808-27-6
5-bromomethyl-3-phenyl-2-trifluoromethyl-thiophene

: 899808-30-1
2-oxo-5-[4-(4-phenyl-5-trifluoromethyl-thiophen-2-ylmethoxy)-phenyl]-pyrrolidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: 96 percent / K₂CO₃ / acetonitrile / 60 °C

2.1: 90 percent / DMAP / CH₂Cl₂ / 20 °C

3.1: LiN(TMS)2 / tetrahydrofuran / -78 °C

3.2: 83 percent / tetrahydrofuran / -78 °C

With dmap; potassium carbonate; lithium hexamethyldisilazane; In tetrahydrofuran; dichloromethane; acetonitrile;
DOI:10.1016/j.bmcl.2006.03.090

Reference yield:

: 899808-28-7
5-[4-(4-phenyl-5-trifluoromethyl-thiophen-2-ylmethoxy)-phenyl]-pyrrolidin-2-one

: 899808-30-1
2-oxo-5-[4-(4-phenyl-5-trifluoromethyl-thiophen-2-ylmethoxy)-phenyl]-pyrrolidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: 90 percent / DMAP / CH₂Cl₂ / 20 °C

2.1: LiN(TMS)2 / tetrahydrofuran / -78 °C

2.2: 83 percent / tetrahydrofuran / -78 °C

With dmap; lithium hexamethyldisilazane; In tetrahydrofuran; dichloromethane;
DOI:10.1016/j.bmcl.2006.03.090