(S)-2-chloro-4-(4-(hydroxymethyl)-2-oxooxazolidin-3-yl)-3-methylbenzonitrile

Base Information

Chemical Name:(S)-2-chloro-4-(4-(hydroxymethyl)-2-oxooxazolidin-3-yl)-3-methylbenzonitrile
CAS No.:1371608-99-9
Molecular Formula:C₁₂H₁₁ClN₂O₃
Molecular Weight:266.684
Hs Code.:

Synonyms:(S)-2-chloro-4-(4-(hydroxymethyl)-2-oxooxazolidin-3-yl)-3-methylbenzonitrile

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Chemical Property of (S)-2-chloro-4-(4-(hydroxymethyl)-2-oxooxazolidin-3-yl)-3-methylbenzonitrile

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Technology Process of (S)-2-chloro-4-(4-(hydroxymethyl)-2-oxooxazolidin-3-yl)-3-methylbenzonitrile

There total 4 articles about (S)-2-chloro-4-(4-(hydroxymethyl)-2-oxooxazolidin-3-yl)-3-methylbenzonitrile 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: 65.0%

: 1371608-98-8
(R)-methyl-3-(3-chloro-4-cyano-2-methylphenyl)-2-oxooxazolidine-4-carboxylate

: 1371608-99-9
(S)-2-chloro-4-(4-(hydroxymethyl)-2-oxooxazolidin-3-yl)-3-methylbenzonitrile

Guidance literature:: With sodium tetrahydroborate; ethanol; at 0 - 20 ℃; for 4h;

Reference yield:

: 796600-15-2
2-chloro-4-fluoro-3-methylbenzonitrile

: 1371608-99-9
(S)-2-chloro-4-(4-(hydroxymethyl)-2-oxooxazolidin-3-yl)-3-methylbenzonitrile

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium carbonate / dimethyl sulfoxide / 12 h / 90 °C

1.2: pH ~ 3

2.1: potassium hydroxide / diethyl ether

2.2: 3 h / 0 °C

3.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 12 h / -78 - 20 °C / Inert atmosphere

4.1: ethanol; sodium tetrahydroborate / 4 h / 0 - 20 °C

With sodium tetrahydroborate; ethanol; potassium carbonate; N-ethyl-N,N-diisopropylamine; potassium hydroxide; In diethyl ether; dichloromethane; dimethyl sulfoxide;

Reference yield:

: 1182367-37-8
(R)-2-(3-chloro-4-cyano-2-methylphenylamino)-3-hydroxypropanoic acid

: 1371608-99-9
(S)-2-chloro-4-(4-(hydroxymethyl)-2-oxooxazolidin-3-yl)-3-methylbenzonitrile

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium hydroxide / diethyl ether

1.2: 3 h / 0 °C

2.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 12 h / -78 - 20 °C / Inert atmosphere

3.1: ethanol; sodium tetrahydroborate / 4 h / 0 - 20 °C

With sodium tetrahydroborate; ethanol; N-ethyl-N,N-diisopropylamine; potassium hydroxide; In diethyl ether; dichloromethane;