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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 380098Generated: October 25, 2026

Benzoin → (5R)-5-(4,5-diphenyloxazol-2-yl)pyrrolidin-2-one

https://huagongshe.com/reaction/380098

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoinHCID 8400—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantD-Pyroglutamic acidHCID 439685—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product(5R)-5-(4,5-diphenyloxazol-2-yl)pyrrolidin-2-oneHCID 54104002—

Reaction Steps

To a solution of D-pyroglutamic acid (30 g) in CH2Cl2 (200 ml) were added benzoin (74 g), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (68 ml) and 4-dimethylaminopyridine (30 g) at room temperature under N2. After being stirred for 12 hours at room temperature, the solvent was evaporated in vacuo, and the residue was partitioned between ethyl acetate and water. The organic layer was washed with 1N-HCl solution, sat. NaHCO3 and brine, dried over MgSO4, and evaporated in vacuo. The obtained compound and ammonium acetate (60 g) were dissolved in acetic acid (500 ml) and the mixture was stirred for 4 hours at 100° C. After the solvent was removed, the residue was partitioned between ethyl acetate and water. The organic layer was washed with water, sat. NaHCO3 and brine. The dried solvent was evaporated in vacuo and the residue was purified by chromatography on silica gel to give (5R)-5-(4,5-diphenyloxazol-2-yl)pyrrolidin-2-one (21.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06300344B1
Source datasetuspto-grants-2001_10
ORD IDord-4711f1f8d222417aacbc503ba9706a33
Source noteuspto-grants-2001_10