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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 380098생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/380098

반응식

참여 물질

역할이름HCID투입량
반응물BenzoinHCID 8400—
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물D-Pyroglutamic acidHCID 439685—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물(5R)-5-(4,5-diphenyloxazol-2-yl)pyrrolidin-2-oneHCID 54104002—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06300344B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-4711f1f8d222417aacbc503ba9706a33
출처 메모uspto-grants-2001_10