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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752944Generated: October 24, 2026

Tetrahydrofuran → (R)-3-(3-Fluorophenyl)-5-(hydroxymethyl)oxazolidin-2-one

https://huagongshe.com/en/reaction/1752944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHexaneHCID 8058—
ReactantAmmonium ChlorideHCID 25517—
Reactant(3-Fluorophenyl)carbamic acid benzyl esterHCID 895321—
ReactantButyllithiumHCID 178418339—
Product(R)-3-(3-Fluorophenyl)-5-(hydroxymethyl)oxazolidin-2-oneHCID 1122959070%

Reaction Conditions

Temperature-78 °C

Reaction Steps

132 g of N-carbobenzyloxy-3-fluoroaniline 132 g prepared in the Preparation example 1 was dissolved in 1.3 L of tetrahydrofuran and the solution was cooled to −78° C. 370 ml of n-buthyllitium (n-BuLi, 1.6M/n-hexane) was slowly added to the solution in a nitrogen atmosphere, followed by stirring for 10 min. And 84 ml of (R)-(−)-glycidylbuthylate was slowly added to the reaction mixture, stirred at the same temperature for 2 hours and allowed to react for 24 hours at room temperature. After completion of the reaction, the solution was added with ammonium chloride (NH4Cl) solution and extracted with 0.5 L of ethyl acetate at room temperature. The organic layer, thus separated, was washed with brine, dried over anhydrous magnesium sulfate and concentrated in vacuo. The residue was dissolved in 100 ml of ethyl acetate and washed with n-hexane to give white crystals, which were purified to the title compound. 80 g. Yield 70%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09163043B2
Source datasetuspto-grants-2015_10
ORD IDord-634994537765496aab4dba73f86e1671
Source noteuspto-grants-2015_10