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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909593Generated: October 30, 2026

2-Oxazolidinone → (R)-4-benzyl-3-((R)-3-(4-(benzyloxy)phenyl)-2-methylpropanoyl)oxazolidin-2-one

https://huagongshe.com/reaction/1909593

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-OxazolidinoneHCID 73949—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant1-(Benzyloxy)-4-(bromomethyl)benzeneHCID 10492756—
Reactant(R)-(-)-4-Benzyl-3-propionyl-2-oxazolidinoneHCID 10966403—
SolventTetrahydrofuranHCID 8028—
Product(R)-4-benzyl-3-((R)-3-(4-(benzyloxy)phenyl)-2-methylpropanoyl)oxazolidin-2-oneHCID 59419856—

Reaction Steps

To a solution of (R)-4-benzyl-3-propionyloxazolidin-2-one (17.0 g, 72.8 mmol) in tetrahydrofuran (200 mL) at −78° C. was added sodium bis(trimethylsilyl)amide (80 mL, 79.4 mmol) and stirred for 1 hour. A solution of 1-(benzyloxy)-4-(bromomethyl)benzene (746) (20.0 g, 72.2 mmol) in tetrahydrofuran (50 mL) was added slowly to the oxazolidinone solution at −78° C. and allowed to warm to room temperature overnight. The solvent was removed in vacuo and the residue was dissolved with ethyl acetate. The organic layer was washed with water, brine, dried over sodium sulfate, filtered, and concentrated in vacuo. The crude compound was purified by flash column chromatography on silica gel with hexanes and EtOAc (20%) to afford (R)-4-benzyl-3-((R)-3-(4-(benzyloxy)phenyl)-2-methylpropanoyl)oxazolidin-2-one (747).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598374B2
Source datasetuspto-grants-2013_12
ORD IDord-fcf01407bb2d492a840e2dfef2f55e38
Source noteuspto-grants-2013_12