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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380124Generated: November 1, 2026

Hydrochloric Acid → HCID 11010755, compound

https://huagongshe.com/reaction/2380124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium ChlorideHCID 5234—
ReactantBenzenepropanoyl chlorideHCID 64801—
Reactant(4S)-4-(propan-2-yl)-1,3-oxazolidin-2-oneHCID 7157133—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 11010755HCID 1101075569,995.297%

Reaction Steps

68.3 ml of butyllithium (as a 1.6M hexane solution) were added dropwise, at -78° C. and under an atmosphere of nitrogen, to a solution of 11.75 g (91.0 mmoles) of 4(S)-isopropyl-2-oxazolidinone in 200 ml of anhydrous tetrahydrofuran. The mixture was stirred for 30 minutes, and then a solution of 18.41 g (0.11 mmoles) of dihydrocinnamoyl chloride in 100 ml of anhydrous tetrahydrofuran was added dropwise over a period of 10 minutes. The mixture was then stirred for a further 1 hour, after which 100 ml of 1N aqueous hydrochloric acid and 100 ml of a saturated aqueous solution of sodium chloride were added to the reaction mixture, which was then extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate, the solvent was removed by distillation under reduced pressure, and the residue was purified by medium pressure silica gel column chromatography (using a 1:4 by volume mixture of ethyl acetate and hexane as eluent), followed by recrystallization from diisopropyl ether, to give 20.12 g (yield 85%) of the title compound as white crystals, melting at 62°-63° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05364844
Source datasetuspto-grants-1994_11
ORD IDord-07e5441e306c406aa4521e855ad10425
Source noteuspto-grants-1994_11