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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638184Generated: November 4, 2026

Hexane → (4S)-4-propan-2-yl-3-prop-2-enoyl-1,3-oxazolidin-2-one

https://huagongshe.com/reaction/1638184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantAcryloyl chlorideHCID 13140—
ReactantAmmonium ChlorideHCID 25517—
Reactant(4S)-4-(propan-2-yl)-1,3-oxazolidin-2-oneHCID 7157133—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(4S)-4-propan-2-yl-3-prop-2-enoyl-1,3-oxazolidin-2-oneHCID 1095418289%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Production in a way similar to: D. A. Evans, K. T. Chapman, J. Bisha J. Am. Chem. Soc. 1988, 110, 1238; A Studer, T. Hintermann, D. Seebach Helv. Chim. Acta 1995, 78, 1185. 6.88 ml of a 1.6M solution of n-BuLi in hexane (11.0 mmol) is slowly added to a solution of 1.299 g (10.0 mmol) of (S)-4-isopropyl-oxazolidin-2-one in 15 ml of absolute THF at -78° C. The solution is stirred for 30 minutes at -78° C.; 1.22 ml (15.0 mmol) of acrylic acid chloride is added drop by drop; it is allowed to reach room temperature and hydrolyzed with 50 ml of saturated NH4Cl solution. It is extracted three times with 50 ml of Et2O each. After drying on MgSO4, the solvent is removed. By flash-chromatographic purification with pentane/Et2O (10:1), 1.63 g (8.9 mmol, 89%) of 20 is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06043372
Source datasetuspto-grants-2000_03
ORD IDord-56cc7c4492014dbdabe389f3f4ebc78a
Source noteuspto-grants-2000_03