돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15187생성일: 2026년 10월 26일

O-(2,4,6-Trimethylbenzenesulfonyl)hydroxylamine → 2-Oxo-octahydrocyclopenta[b]pyrrol-4-yl benzoate

https://huagongshe.com/reaction/15187

반응식

참여 물질

역할이름HCID투입량
반응물O-(2,4,6-Trimethylbenzenesulfonyl)hydroxylamineHCID 11830845—
반응물6-Oxobicyclo[3.2.0]heptan-2-yl benzoateHCID 59259575—
용매DichloromethaneHCID 6344—
생성물1-Oxo-octahydrocyclopenta[c]pyrrol-4-yl benzoateHCID 59259560—
생성물2-Oxo-octahydrocyclopenta[b]pyrrol-4-yl benzoateHCID 59259571133.4%

반응 단계

To a stirred solution of compound 1H (500 mg, 2.2 mmol) in CH2Cl2 (5 mL) was added a solution of O-mesitylenesulfonylhydroxylamine (650 mg, 3 mmol) in CH2Cl2 (2 mL) at −10° C., and the stirring was continued for 20 min between −10 to 0° C. It was concentrated, added to a mixed solvent of benzene and methanol (30 mL, 3:1) followed by a slurry of basic alumina (25 g) in methanol (20 mL). The reaction mixture was stirred at RT overnight, and alumina solid was removed by filtration. Purification by silica gel chromatography (5% to 100% EtOAc in hexanes, then 5% methanol in EtOAc) provide mixtures of the title compounds 1I and 1J (total 360 mg) as a yellow oil. MS (ES) m/z 246 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732480B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-69d09e97128d4e6b92c02884fe908ded
출처 메모uspto-grants-2010_06