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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695026Generated: November 2, 2026

Hexane → (S)-4-benzyl-3-pentanoyloxazolidin-2-one

https://huagongshe.com/reaction/1695026

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantAmmonium ChlorideHCID 25517—
ReactantValeryl chlorideHCID 61186—
Reactant(S)-4-Benzyl-2-oxazolidinoneHCID 736225—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(S)-4-benzyl-3-pentanoyloxazolidin-2-oneHCID 11391341101.2%

Reaction Steps

90 ml of a solution of n-butyllithium in n-hexane (1.60 mol/l) (144 mmol) was added to a solution of 25.0 g of (S)-4-benzyl-2-oxazolidinone (141 mmol) in tetrahydrofuran (600 ml) under a nitrogen atmosphere and at −78° C. over 10 minutes, and the mixture was stirred at the same temperature for 20 minutes. Then, 19.0 ml of n-valeryl chloride (159 mmol) was added over 10 minutes. The mixture was stirred at the same temperature for 20 minutes and then further stirred at room temperature for three hours. 90 ml of a saturated ammonium chloride aqueous solution was added to the reaction mixture, and the mixture was further stirred at room temperature for 15 minutes. The reaction mixture was concentrated under reduced pressure and diluted with 300 ml of water, followed by extraction with methylene chloride. Then, the organic layer was washed with a saturated sodium bicarbonate aqueous solution and brine and dried over anhydrous magnesium sulfate. After filtration, the solvent was evaporated under reduced pressure to obtain 37.3 g of the crude title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158790B2
Source datasetuspto-grants-2012_04
ORD IDord-02c4a897613648eb8bbe3f42e35cd3bf
Source noteuspto-grants-2012_04