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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230142Generated: November 1, 2026

Water → HCID 59902314, compound

https://huagongshe.com/reaction/2230142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
Reactant(4R)-4-phenyl-1,3-oxazolidin-2-oneHCID 730425—
ReactantButyllithiumHCID 178418339—
SolventChloroformHCID 6212—
ProductHCID 59902314HCID 59902314—

Reaction Conditions

Temperature0 °C

Reaction Steps

4-(R)-Phenyloxazolidin-2-one (33.0 g, 0.202 mol) was dissolved in THF (1 L) and cooled to −78° C. n-Butyl lithium (2.5 M in hexanes, 79.5 mL, 0.198 mol) was added, and the resulting reaction mixture was stirred for 20 minutes. A solution of Intermediate 62 (65.1 g, 0.213 mol) in THF (200 mL) was added dropwise over 15 minutes. The reaction mixture was stirred for 1 hour at −78° C., then warmed to 0° C., slowly. The reaction mixture became thick with beige solids. The mixture was neutralized at 0° C. with saturated NH4Cl (600 mL) and water (300 mL). The solution was warmed to 22° C. quickly and poured into CHCl3 (2400 mL). After shaking and separation, the organic layer was washed with water (1 L), saturated NaCl (1 L), dried over Na2SO4, and concentrated in vacuo to a pale orange solid (94.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06423710B1
Source datasetuspto-grants-2002_07
ORD IDord-e1fe824e8e4a4d70b6fbd8a9eade2dcb
Source noteuspto-grants-2002_07