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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269212Generated: October 31, 2026

Acetaldehyde → 2-(3,4-Difluorophenyl)-3-methyl-3-hydroxypropionic acid

https://huagongshe.com/reaction/2269212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
Reactant(3,4-Difluorophenyl)acetic acidHCID 69571—
ReactantLithium diisopropylamideHCID 2724682—
Reactant4(S)-(3,4-difluorophenyl)-5(S)-methyloxazolidin-2-oneHCID 10512750—
Product2-(3,4-Difluorophenyl)-3-methyl-3-hydroxypropionic acidHCID 11481333—

Reaction Steps

4(S)-(3,4-difluorophenyl)-5(S)-methyloxazolidin-2-one precursor to Compound A can be prepared by treating 3,4-difluorophenylacetic acid with LDA, followed by reaction with acetaldehyde to form 2-(3,4-difluorophenyl)-3-methyl-3-hydroxypropionic acid, and then cyclizing the hydroxypropionic acid with diphenyldiphosphorylazide to form the oxazolidinone. The oxazolidinone can then be activated by treatment with p-nitrophenylchloroformate. The oxazolidinones can be resolved into their optical isomers via chromatography prior to activation, or the unresolved material can be activated directly. The activated oxazolidinone is then acylated to give Compound A by treatment with 3-[4-(4-fluorophenyl)piperidin-1-yl]propylamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329393B1
Source datasetuspto-grants-2001_12
ORD IDord-87a5df08da08400ea63eb766a28cd78a
Source noteuspto-grants-2001_12