2,5-dioxo-4-(4-trifluoromethyl-phenyl)-oxazolidine-3-carboxylic acid benzyl ester

Base Information

• Chemical Name: 2,5-dioxo-4-(4-trifluoromethyl-phenyl)-oxazolidine-3-carboxylic acid benzyl ester
• CAS No.: 470670-68-9
• Molecular Formula: C₁₈H₁₂F₃NO₅
• Molecular Weight: 379.292
• Mol file: 470670-68-9.mol

Synonyms:2,5-dioxo-4-(4-trifluoromethyl-phenyl)-oxazolidine-3-carboxylic acid benzyl ester

Chemical Property of 2,5-dioxo-4-(4-trifluoromethyl-phenyl)-oxazolidine-3-carboxylic acid benzyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2,5-dioxo-4-(4-trifluoromethyl-phenyl)-oxazolidine-3-carboxylic acid benzyl ester

There total 2 articles about 2,5-dioxo-4-(4-trifluoromethyl-phenyl)-oxazolidine-3-carboxylic acid benzyl 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:

4-(4-trifluoromethyl-phenyl)-oxazolidine-2,5-dione + benzyl chloroformate (501-53-1,94274-21-2) → 2,5-dioxo-4-(4-trifluoromethyl-phenyl)-oxazolidine-3-carboxylic acid benzyl ester (470670-68-9)

Guidance literature:

With 4-methyl-morpholine; In tetrahydrofuran; at -25 - 20 ℃;

DOI:10.1021/ol026660l

Reference yield:

2-amino-2-[4-(trifluoromethyl)phenyl]acetic acid (144789-73-1,144789-75-3,142012-65-5) → 2,5-dioxo-4-(4-trifluoromethyl-phenyl)-oxazolidine-3-carboxylic acid benzyl ester (470670-68-9)

Guidance literature:

Multi-step reaction with 2 steps

1: tetrahydrofuran / 3 h / 50 °C

2: N-methyl-morpholine / tetrahydrofuran / -25 - 20 °C

With 4-methyl-morpholine; In tetrahydrofuran;

DOI:10.1021/ol026660l

Reference yield:

allyl alcohol (107-18-6) + 2,5-dioxo-4-(4-trifluoromethyl-phenyl)-oxazolidine-3-carboxylic acid benzyl ester (470670-68-9) → (+)-allyl-(N-benzyloxycarbonyl)-p-trifluoromethylphenylglycinate + (-)-allyl-(N-benzyloxycarbonyl)-p-trifluoromethyl-phenylglycinate

Guidance literature:

With hydroquinidine anthraquinone-1,4-diyl diether; 4 A molecular sieve; In diethyl ether; at 23 ℃; for 1h; Title compound not separated from byproducts.;

DOI:10.1021/ol026660l

upstream raw materials:

benzyl chloroformate

2-amino-2-[4-(trifluoromethyl)phenyl]acetic acid