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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1595495생성일: 2026년 10월 27일

3-Nitrobenzenesulfonyl chloride → 4-(Tert-butoxycarbonylamino)phenethyl 3-nitro-benzenesulfonate

https://huagongshe.com/reaction/1595495

반응식

참여 물질

역할이름HCID투입량
반응물3-Nitrobenzenesulfonyl chlorideHCID 8476—
반응물N-Boc-2-(4-aminophenyl)ethanolHCID 11413715—
용매DichloromethaneHCID 6344—
생성물4-(Tert-butoxycarbonylamino)phenethyl 3-nitro-benzenesulfonateHCID 5453544247%

반응 조건

온도-25 °C

반응 단계

2-[4-(tert-butoxycarbonylamino)phenyl]-1-ethanol dissolved in dichloromethane. The reaction mixture was cooled to −25° C. and 9.34 g (42 mmole) 3-nitrobenzenesulfonyl chloride was added in portions. The reaction mixture was poured on to icewater, the phases were separated and the organic phase was dried (sodium sulfate), filtered and the solvent was evaporated in vacuo. The residue was purified by chromatography on silica gel using dichloromethane as eluent to give 8.3 g (yield 47%) 4-(tert-butoxycarbonylamino)-phenethyl 3-nitro-benzenesulfonate as yellow crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06288096B1
출처 데이터셋uspto-grants-2001_09
ORD IDord-79a2174653aa4d7689200bc2493fb569
출처 메모uspto-grants-2001_09