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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 65439생성일: 2026년 10월 23일

Potassium Phosphate, Dibasic → 3-(S)-hydroxymethyl-4-(R)-tert.-butylsulphonyl-2-azetidinone

https://huagongshe.com/ko/reaction/65439

반응식

참여 물질

역할이름HCID투입량
반응물Potassium Phosphate, DibasicHCID 24450—
반응물Sodium PersulfateHCID 62655—
반응물1-p-methoxybenzyl-3-(S)-hydroxymethyl-4-(R)-tert.-butylsulphonyl-2-azetidinoneHCID 18604772—
촉매Ferrous sulfate heptahydrateHCID 62662—
촉매Cupric acetate monohydrateHCID 165397—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물3-(S)-hydroxymethyl-4-(R)-tert.-butylsulphonyl-2-azetidinoneHCID 18604774—

반응 단계

A solution of 68.3 mg (0.2 mmol) of 1-p-methoxybenzyl-3-(S)-hydroxymethyl-4-(R)-tert.-butylsulphonyl-2-azetidinone in 4 ml of acetonitrile is added to a solution of 428 mg (1.8 mmol) of sodium peroxydisulphate, 174 mg (1 mmol) of dipotassium hydrogen phosphate, 1 mg of iron(II) sulphate heptahydrate and 2 mg of copper(II) acetate hydrate in 4 ml of water. The mixture is stirred for 2 hours under an argon atmosphere at a bath temperature of 65°. The resulting mixture is then concentrated to half its volume under reduced pressure and extracted with ethyl acetate. The extract is triturated with methylene chloride and ether and the pure title compound is obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04614614
출처 데이터셋uspto-grants-1986_09
ORD IDord-139ed6457cd64e2e9fcb010d4805aeea
출처 메모uspto-grants-1986_09