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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 380123Generated: October 30, 2026

(2S)-2-(4,5-diphenyloxazol-2-yl)oxirane → (4S)-4-(4,5-diphenyloxazol-2-yl)-4-hydroxy-1-butene

https://huagongshe.com/reaction/380123

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S)-2-(4,5-diphenyloxazol-2-yl)oxiraneHCID 57131304—
ReactantHCID 178461836HCID 178461836—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTetrahydrofuranHCID 8028—
Product(4S)-4-(4,5-diphenyloxazol-2-yl)-4-hydroxy-1-buteneHCID 56991674—

Reaction Steps

To a solution of (2S)-2-(4,5-diphenyloxazol-2-yl)oxirane (12 g) and CuI (0.19 g) in THF (240 ml) was dropwise added a solution of vinylmagnesium chloride in THF (1.0M solution, 101 ml) at −78° C. under N2. The mixture was stirred for 1 hour at room temperature and partitioned between ethyl acetate and water. The organic layer was washed with 1N-HCl, water, sat. NaHCO3 and brine. The dried solvent was evaporated in vacuo and the residue was purified by chromatography on silica gel to give (4S)-4-(4,5-diphenyloxazol-2-yl)-4-hydroxy-1-butene (9.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06300344B1
Source datasetuspto-grants-2001_10
ORD IDord-525d6f3f68c34670aa445f84667745bc
Source noteuspto-grants-2001_10