(S)-2-(5,5-bis(4-fluorophenyl)-2-oxo-4-phenyloxazolidin-3-yl)acetic acid

Base Information

Chemical Name:(S)-2-(5,5-bis(4-fluorophenyl)-2-oxo-4-phenyloxazolidin-3-yl)acetic acid
CAS No.:1609284-94-7
Molecular Formula:C₂₃H₁₇F₂NO₄
Molecular Weight:409.389
Hs Code.:

Synonyms:(S)-2-(5,5-bis(4-fluorophenyl)-2-oxo-4-phenyloxazolidin-3-yl)acetic acid

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Chemical Property of (S)-2-(5,5-bis(4-fluorophenyl)-2-oxo-4-phenyloxazolidin-3-yl)acetic acid

Chemical Property:

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Technology Process of (S)-2-(5,5-bis(4-fluorophenyl)-2-oxo-4-phenyloxazolidin-3-yl)acetic acid

There total 4 articles about (S)-2-(5,5-bis(4-fluorophenyl)-2-oxo-4-phenyloxazolidin-3-yl)acetic 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: 100.0%

: 1609284-93-6
(S)-ethyl 2-(5,5-bis(4-fluorophenyl)-2-oxo-4-phenyloxazolidin-3-yl)acetate

: 1609284-94-7
(S)-2-(5,5-bis(4-fluorophenyl)-2-oxo-4-phenyloxazolidin-3-yl)acetic acid

Guidance literature:: With water; sodium hydroxide; In ethanol; for 0.25h;

Reference yield:

: 1609284-92-5
(S)-5,5-bis(4-fluorophenyl)-4-phenyloxazolidin-2-one

: 1609284-94-7
(S)-2-(5,5-bis(4-fluorophenyl)-2-oxo-4-phenyloxazolidin-3-yl)acetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydride / tetrahydrofuran; mineral oil / 20 °C / Cooling with ice

2: sodium hydroxide; water / ethanol / 0.25 h

With water; sodium hydride; sodium hydroxide; In tetrahydrofuran; ethanol; mineral oil;

Reference yield:

: 1609284-91-4
(S)-2-amino-1,1-bis(4-fluorophenyl)-2-phenylethanol

: 1609284-94-7
(S)-2-(5,5-bis(4-fluorophenyl)-2-oxo-4-phenyloxazolidin-3-yl)acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / dichloromethane / 20 °C / Cooling with ice

2: sodium hydride / tetrahydrofuran; mineral oil / 20 °C / Cooling with ice

3: sodium hydroxide; water / ethanol / 0.25 h

With water; sodium hydride; triethylamine; sodium hydroxide; In tetrahydrofuran; ethanol; dichloromethane; mineral oil;