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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 451673생성일: 2026년 10월 24일

(R)-tert-butyl 3-((R)-(2-(tert-butyldimethylsilyloxy)ethoxy)(3-chlorophenyl)methyl)piperidine-1-carboxylate → 2-((R)-(3-chlorophenyl)((R)-piperidin-3-yl)methoxy)ethanol

https://huagongshe.com/ko/reaction/451673

반응식

참여 물질

역할이름HCID투입량
반응물(R)-tert-butyl 3-((R)-(2-(tert-butyldimethylsilyloxy)ethoxy)(3-chlorophenyl)methyl)piperidine-1-carboxylateHCID 59201708—
용매Hydrochloric AcidHCID 313—
용매AcetonitrileHCID 6342—
생성물2-((R)-(3-chlorophenyl)((R)-piperidin-3-yl)methoxy)ethanolHCID 59201741—

반응 단계

A solution of crude (R)-tert-butyl 3-((R)-(2-(tert-butyldimethylsilyloxy)ethoxy)(3-chlorophenyl)methyl)piperidine-1-carboxylate in CH3CN (100 mL) and 2 N aq HCl (100 mL) was vigorously stirred at rt for 2 d. The solvents were removed in vacuo to give the HCl salt of 2-((R)-(3-chlorophenyl)((R)-piperidin-3-yl)methoxy)ethanol, which was used in the next step without further purification. LC-MS (3 min) tR=1.05 min m/z 272, 270 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08487108B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-5b404a4e2a6445a599aa7c2199b939f4
출처 메모uspto-grants-2013_07