(R)-1-(4-(2-(4-trifluoromethylphenyl)oxazol-4-ylmethoxy)benzyl)pyrrolidine-2-carboxylic acid

Base Information

Chemical Name:(R)-1-(4-(2-(4-trifluoromethylphenyl)oxazol-4-ylmethoxy)benzyl)pyrrolidine-2-carboxylic acid
CAS No.:1065335-10-5
Molecular Formula:C₂₃H₂₁F₃N₂O₄
Molecular Weight:446.426
Hs Code.:

Synonyms:(R)-1-(4-(2-(4-trifluoromethylphenyl)oxazol-4-ylmethoxy)benzyl)pyrrolidine-2-carboxylic acid

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Chemical Property of (R)-1-(4-(2-(4-trifluoromethylphenyl)oxazol-4-ylmethoxy)benzyl)pyrrolidine-2-carboxylic acid

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Technology Process of (R)-1-(4-(2-(4-trifluoromethylphenyl)oxazol-4-ylmethoxy)benzyl)pyrrolidine-2-carboxylic acid

There total 6 articles about (R)-1-(4-(2-(4-trifluoromethylphenyl)oxazol-4-ylmethoxy)benzyl)pyrrolidine-2-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: 60.0%

: 1065335-12-7
(R)-1-(4-(2-(4-trifluoromethylphenyl)oxazol-4-ylmethoxy)benzyl)pyrrolidine-2-carboxylic acid methyl ester

: 1065335-10-5
(R)-1-(4-(2-(4-trifluoromethylphenyl)oxazol-4-ylmethoxy)benzyl)pyrrolidine-2-carboxylic acid

Guidance literature:: (R)-1-(4-(2-(4-trifluoromethylphenyl)oxazol-4-ylmethoxy)benzyl)pyrrolidine-2-carboxylic acid methyl ester; With lithium hydroxide; water; In methanol; at 20 ℃; for 48h;

With hydrogenchloride; In methanol; water;

Reference yield:

: 123-08-0,65581-83-1
4-hydroxy-benzaldehyde

: 1065335-10-5
(R)-1-(4-(2-(4-trifluoromethylphenyl)oxazol-4-ylmethoxy)benzyl)pyrrolidine-2-carboxylic acid

Guidance literature:: Multi-step reaction with 5 steps

1: potassium carbonate / N,N-dimethyl-formamide / 3 h / 90 °C

2: sodium tetrahydroborate / methanol / 1 h / 20 °C

3: methanesulfonyl chloride; triethylamine / dichloromethane / 3 h / 20 °C

4: potassium carbonate / N,N-dimethyl-formamide / 3 h / 20 °C

5: lithium hydroxide; water / methanol / 48 h / 20 °C

With lithium hydroxide; sodium tetrahydroborate; water; potassium carbonate; methanesulfonyl chloride; triethylamine; In methanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1065333-91-6
4-(4-chloromethylphenoxymethyl)-2-(4-trifluoromethylphenyl)oxazole

: 1065335-10-5
(R)-1-(4-(2-(4-trifluoromethylphenyl)oxazol-4-ylmethoxy)benzyl)pyrrolidine-2-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / N,N-dimethyl-formamide / 3 h / 20 °C

2: lithium hydroxide; water / methanol / 48 h / 20 °C

With lithium hydroxide; water; potassium carbonate; In methanol; N,N-dimethyl-formamide;