((2R,4S)-3-Benzoyl-4-benzyl-5-oxo-2-phenyl-oxazolidin-4-yl)-acetyl chloride

Base Information

Chemical Name:((2R,4S)-3-Benzoyl-4-benzyl-5-oxo-2-phenyl-oxazolidin-4-yl)-acetyl chloride
CAS No.:179910-98-6
Molecular Formula:C₂₅H₂₀ClNO₄
Molecular Weight:433.891
Hs Code.:

Synonyms:((2R,4S)-3-Benzoyl-4-benzyl-5-oxo-2-phenyl-oxazolidin-4-yl)-acetyl chloride

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of ((2R,4S)-3-Benzoyl-4-benzyl-5-oxo-2-phenyl-oxazolidin-4-yl)-acetyl chloride

Chemical Property:

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Technology Process of ((2R,4S)-3-Benzoyl-4-benzyl-5-oxo-2-phenyl-oxazolidin-4-yl)-acetyl chloride

There total 3 articles about ((2R,4S)-3-Benzoyl-4-benzyl-5-oxo-2-phenyl-oxazolidin-4-yl)-acetyl chloride 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:

: 179910-97-5
((2'R,4'S)-(+)-3'-Benzoyl-4'-benzyl-5'-oxo-2'-phenyloxazolidin-4'-yl)acetic acid

: 179910-98-6
((2R,4S)-3-Benzoyl-4-benzyl-5-oxo-2-phenyl-oxazolidin-4-yl)-acetyl chloride

Guidance literature:: With oxalyl dichloride; In dichloromethane; N,N-dimethyl-formamide; 1.) 0 deg C, 2 h, 2.) 20 deg C, 16 h;
DOI:10.1039/P19960001299

Reference yield:

: 113806-30-7
(2R,4S)-3-benzoyl-4-benzyl-2-phenyloxazolidin-5-one

: 179910-98-6
((2R,4S)-3-Benzoyl-4-benzyl-5-oxo-2-phenyl-oxazolidin-4-yl)-acetyl chloride

Guidance literature:: Multi-step reaction with 3 steps

1.1: LiHMDS / tetrahydrofuran / 0.12 h / -78 °C

1.2: 87 percent / tetrahydrofuran / -78 - 20 °C

2.1: 41 percent / TFA / CH₂Cl₂ / 0.08 h / 0 °C

3.1: oxalyl chloride; dimethylformamide / CH₂Cl₂ / 0 - 20 °C

With oxalyl dichloride; N,N-dimethyl-formamide; trifluoroacetic acid; lithium hexamethyldisilazane; In tetrahydrofuran; dichloromethane; 1.1: Metallation / 1.2: Alkylation / 2.1: Hydrolysis / 3.1: Chlorination;
DOI:10.1021/jo991306v

Reference yield:

: 258854-42-1
(2R,4S)-tert-butyl 3-benzoyl-4-benzyl-5-oxo-2-phenyl-1,3-oxazolidin-4-yl ethanoate

: 179910-98-6
((2R,4S)-3-Benzoyl-4-benzyl-5-oxo-2-phenyl-oxazolidin-4-yl)-acetyl chloride

Guidance literature:: Multi-step reaction with 2 steps

1: 41 percent / TFA / CH₂Cl₂ / 0.08 h / 0 °C

2: oxalyl chloride; dimethylformamide / CH₂Cl₂ / 0 - 20 °C

With oxalyl dichloride; N,N-dimethyl-formamide; trifluoroacetic acid; In dichloromethane; 1: Hydrolysis / 2: Chlorination;
DOI:10.1021/jo991306v