돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 65437생성일: 2026년 10월 23일

Potassium Persulfate → 3-(S)-hydroxymethyl-4-(R)-tert.-butylsulphonyl-2-azetidinone

https://huagongshe.com/ko/reaction/65437

반응식

참여 물질

역할이름HCID투입량
반응물Potassium PersulfateHCID 24412—
반응물Potassium Phosphate, DibasicHCID 24450—
반응물1-(2,4-dimethoxybenzyl)-3-(S)-hydroxymethyl-4-(R)-tert.butylsulphonyl-2-azetidinoneHCID 18604771—
용매AcetonitrileHCID 6342—
생성물3-(S)-hydroxymethyl-4-(R)-tert.-butylsulphonyl-2-azetidinoneHCID 18604774—

반응 단계

A solution of 74 mg (0.2 mmol) of 1-(2,4-dimethoxybenzyl)-3-(S)-hydroxymethyl-4-(R)-tert.butylsulphonyl-2-azetidinone (see Example 20), 486 mg (1.8 mmol) of potassium peroxydisulphate and 174 mg (1.0 mmol) of dipotassium hydrogen phosphate in 4 ml of acetonitrile is stirred for 2 hours at 65° under a reflux condenser, the resulting reaction mixture is freed from acetonitrile under reduced pressure and the aqueous residue is extracted with ethyl acetate. After drying of the organic phase over Na2SO4 and concentration by evaporation in vacuo, a residue is obtained from which the title compound is obtained in the form of colourless crystals by adding a little methylene chloride and ether.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04614614
출처 데이터셋uspto-grants-1986_09
ORD IDord-aa853de2f5c04505a7cd89b5973f20c2
출처 메모uspto-grants-1986_09