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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911521Generated: October 30, 2026

(R)-Tert-butyl 4-acetyl-2,2-dimethyloxazolidine-3-carboxylate → HCID 68714982, compound

https://huagongshe.com/reaction/1911521

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-Tert-butyl 4-acetyl-2,2-dimethyloxazolidine-3-carboxylateHCID 10977654—
ReactantHCID 178418336HCID 178418336—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68714982HCID 6871498289%

Reaction Steps

A solution of (R)-4-acetyl-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (2.80 g, CAS 167102-63-8) in THF (40 ml) was cooled under an argon atmosphere to 0° C. and treated dropwise with benzylmagnesium chloride solution (1 M in diethylether, 34.5 ml). The reaction mixture was stirred at r.t. overnight, then quenched with saturated aqueous NH4Cl (50 ml) and extracted with EtOAc. The organic layer was washed with H2O and brine, dried over MgSO4, filtered and concentrated. The crude product was purified by column chromatography (silica gel; gradient: cyclohexane ->cyclohexane/EtOAc 3:1) to give (R)-4-(1-hydroxy-1-methyl-2-phenyl-ethyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (3.45 g, 89%) as off-white waxy solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604061B2
Source datasetuspto-grants-2013_12
ORD IDord-b63b63a03c6247b786ea3d647a2914ca
Source noteuspto-grants-2013_12