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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365581Generated: October 30, 2026

Sodium Bicarbonate → 2-Propanol, 2-methyl-, lithium salt (1:1)

https://huagongshe.com/reaction/1365581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant(2R)-Oxiran-2-ylmethyl butanoateHCID 2724536—
ReactantHCID 22716470HCID 22716470—
ReactantButyllithiumHCID 178418339—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
SolventTetrahydrofuranHCID 8028—
Product2-Propanol, 2-methyl-, lithium salt (1:1)HCID 23664764—
ProductHCID 54327468HCID 54327468—

Reaction Steps

A solution of lithium t-butoxide is prepared by addition of n-butyllithium (1.6 M in hexane, 2.9 ml) to a stirred solution of t-butanol (0.43 g) in anhydrous THF (10 ml) at −10° under argon. After cooling to −70°, a solution of 5-benzyloxycarbonylamino-2-(4-[2-fluoroethyl]-3-oxopiperazin-1-yl)fluorobenzene (1.5 g) in dry THF (15 ml) is added. After 10 minutes, (R)-glycidylbutyrate (0.67 g) in dry THF (15 ml) is added to the resulting mixture, and stirring continued at −70° for 15 minutes, before allowing the temperature to rise to 20–25° over 16 hours. Methanol (10 ml) is added, followed by saturated sodium bicarbonate solution (20 ml) and water (10 ml). The organic phase is separated and extracted into ethyl acetate (3×25 ml), washed with saline and dried over magnesium sulfate. The solvent is removed and the residue purified by chromatography (silica; eluting with a gradient increasing in polarity from 0 to 3% methanol in dichloromethane) to give (5R)-3-(3-fluoro-4-[4-(2-fluoroethyl)-3-oxopiperazin-1-yl]phenyl)-5-hydroxymethyloxazolidin-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07892574B2
Source datasetuspto-grants-2011_02
ORD IDord-952f55fc9b4a48f591eb53fc044730a4
Source noteuspto-grants-2011_02