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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 382779생성일: 2026년 10월 26일

4-Benzylpiperidine → 4[-2-(4-Benzyl-piperidine-1-yl)-ethanesulfonyl]-phenol

https://huagongshe.com/reaction/382779

반응식

참여 물질

역할이름HCID투입량
반응물4-BenzylpiperidineHCID 31738—
반응물4-(2-Chloro-ethanesulfonyl)-phenolHCID 9813249—
용매DichloromethaneHCID 6344—
생성물4[-2-(4-Benzyl-piperidine-1-yl)-ethanesulfonyl]-phenolHCID 979894538.7%

반응 단계

To a solution of 40.0 g 4-(2-chloro-ethanesulfonyl)-phenol (181 mmol) in 600 ml CH2Cl2 were added 69.9 g 4-benzylpiperidine (399 mmol). After stirring for 16 h at r. t. the reaction mixture was concentrated to 100 ml and directly purified by chromatography over silica gel (CH2Cl2/MeOH/NH3 19/1/0.1). Recrystallization from ethyl acetatelhexane (2:1) yielded 25 g product (70 mmol, 38%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06310213B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-840af965b37549a1b786c559c48d75aa
출처 메모uspto-grants-2001_10