(2R,4R)-2-benzyl-3-[(E)-4,4,4-trifluoro-3-oxobut-1-enyl]thiazolidine-4-carboxylic acid

Base Information

Chemical Name:(2R,4R)-2-benzyl-3-[(E)-4,4,4-trifluoro-3-oxobut-1-enyl]thiazolidine-4-carboxylic acid
CAS No.:1430843-61-0
Molecular Formula:C₁₅H₁₄F₃NO₃S
Molecular Weight:345.342
Hs Code.:

Synonyms:(2R,4R)-2-benzyl-3-[(E)-4,4,4-trifluoro-3-oxobut-1-enyl]thiazolidine-4-carboxylic acid

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Chemical Property of (2R,4R)-2-benzyl-3-[(E)-4,4,4-trifluoro-3-oxobut-1-enyl]thiazolidine-4-carboxylic acid

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Technology Process of (2R,4R)-2-benzyl-3-[(E)-4,4,4-trifluoro-3-oxobut-1-enyl]thiazolidine-4-carboxylic acid

There total 1 articles about (2R,4R)-2-benzyl-3-[(E)-4,4,4-trifluoro-3-oxobut-1-enyl]thiazolidine-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: 84.0%

: 50739-30-5
2-benzyl-1,3-thiazolidine-4-carboxylic acid

: 59938-06-6,17129-06-5
4-ethoxy-1,1,1-trifluoro-3-butene-2-one

: 1430843-61-0
(2R,4R)-2-benzyl-3-[(E)-4,4,4-trifluoro-3-oxobut-1-enyl]thiazolidine-4-carboxylic acid

Guidance literature:: In acetonitrile; at 60 ℃; for 24h;
DOI:10.1016/j.tet.2013.03.017

Reference yield: 76.0%

: 1430843-61-0
(2R,4R)-2-benzyl-3-[(E)-4,4,4-trifluoro-3-oxobut-1-enyl]thiazolidine-4-carboxylic acid

: 407-25-0
trifluoroacetic anhydride

: 1430843-62-1
(R)-3-benzyl-7-trifluoromethyl-1H,3H-pyrrolo[1,2-c]thiazole

Guidance literature:: In dichloromethane; at 0 - 20 ℃; for 8h;
DOI:10.1016/j.tet.2013.03.017

Reference yield:

: 1430843-61-0
(2R,4R)-2-benzyl-3-[(E)-4,4,4-trifluoro-3-oxobut-1-enyl]thiazolidine-4-carboxylic acid

: 1430843-63-2
3-benzyl-7-trifluoromethyl-1H,3H-pyrrolo[1,2-c]thiazole-2,2-dioxide

Guidance literature:: Multi-step reaction with 2 steps

1: dichloromethane / 8 h / 0 - 20 °C

2: sodium tungstate (VI) dihydrate; phenylphosphonate; Aliquat 336; dihydrogen peroxide / ethyl acetate; water / 144 h / 40 °C

With sodium tungstate (VI) dihydrate; phenylphosphonate; dihydrogen peroxide; Aliquat 336; In dichloromethane; water; ethyl acetate;
DOI:10.1016/j.tet.2013.03.017