(2S,4R)-4-Benzyl-2-biphenyl-4-yl-4-methyl-5-oxo-oxazolidine-3-carboxylic acid isobutyl ester

Base Information

Chemical Name:(2S,4R)-4-Benzyl-2-biphenyl-4-yl-4-methyl-5-oxo-oxazolidine-3-carboxylic acid isobutyl ester
CAS No.:346578-00-5
Molecular Formula:C₂₈H₂₉NO₄
Molecular Weight:443.543
Hs Code.:

Synonyms:(2S,4R)-4-Benzyl-2-biphenyl-4-yl-4-methyl-5-oxo-oxazolidine-3-carboxylic acid isobutyl ester

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Chemical Property of (2S,4R)-4-Benzyl-2-biphenyl-4-yl-4-methyl-5-oxo-oxazolidine-3-carboxylic acid isobutyl ester

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Technology Process of (2S,4R)-4-Benzyl-2-biphenyl-4-yl-4-methyl-5-oxo-oxazolidine-3-carboxylic acid isobutyl ester

There total 6 articles about (2S,4R)-4-Benzyl-2-biphenyl-4-yl-4-methyl-5-oxo-oxazolidine-3-carboxylic acid isobutyl 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: 100.0%

: 100-39-0
benzyl bromide

: 346577-99-9
(2S,4S)-2-(biphenyl-4-yl)-4-methyl-5-oxo-oxazolidine-3-carboxylic acid isobutyl ester

: 346578-00-5
(2S,4R)-4-Benzyl-2-biphenyl-4-yl-4-methyl-5-oxo-oxazolidine-3-carboxylic acid isobutyl ester

Guidance literature:: With lithium hexamethyldisilazane; In tetrahydrofuran; hexane; at -27 ℃;
DOI:10.1016/S0040-4039(01)00403-8

Reference yield:

: 183140-29-6
N-isobutyloxycarbonyl-(S)-alanine

: 346578-00-5
(2S,4R)-4-Benzyl-2-biphenyl-4-yl-4-methyl-5-oxo-oxazolidine-3-carboxylic acid isobutyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: oxalyl chloride; DMF / CH₂Cl₂ / 5 h / 20 °C

2: 92 percent / SnCl₄ / CH₂Cl₂ / 20 h / 25 °C

3: LiHMDS / tetrahydrofuran / 3.5 h / -25 - 20 °C

With oxalyl dichloride; tin(IV) chloride; N,N-dimethyl-formamide; lithium hexamethyldisilazane; In tetrahydrofuran; dichloromethane;
DOI:10.2533/chimia.2006.566

Reference yield:

: 3218-36-8
4-Phenylbenzaldehyde

: 346578-00-5
(2S,4R)-4-Benzyl-2-biphenyl-4-yl-4-methyl-5-oxo-oxazolidine-3-carboxylic acid isobutyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 91 percent / p-TsOH / cyclohexane / 18 h / Heating

2: 100 percent / LiN(SiMe₃)2 / tetrahydrofuran; hexane / -27 °C

With toluene-4-sulfonic acid; lithium hexamethyldisilazane; In tetrahydrofuran; hexane; cyclohexane;
DOI:10.1016/S0040-4039(01)00403-8