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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 380124Generated: October 31, 2026

Phthalimide → (4R)-4-(4,5-diphenyloxazol-2-yl)-4-phthalimido-1-butene

https://huagongshe.com/reaction/380124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalimideHCID 6809—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant(4S)-4-(4,5-diphenyloxazol-2-yl)-4-hydroxy-1-buteneHCID 56991674—
SolventTetrahydrofuranHCID 8028—
Product(4R)-4-(4,5-diphenyloxazol-2-yl)-4-phthalimido-1-buteneHCID 5455830973.1%

Reaction Steps

To a solution of (4S)-4-(4,5-diphenyloxazol-2-yl)-4-hydroxy-1-butene (9.2 g) in THF (100 ml) were added phthalimide (7.0 g) and triphenylphosphine (12.5 g) and diethyl azodiformate (7.5 ml) at room temperature. The mixture was stirred for 2 hours 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 (4R)-4-(4,5-diphenyloxazol-2-yl)-4-phthalimido-1-butene (9.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06300344B1
Source datasetuspto-grants-2001_10
ORD IDord-97ba460a673340e3b106d8b58027faaa
Source noteuspto-grants-2001_10