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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1060806생성일: 2026년 10월 27일

Acetic Acid → tert-Butyl 4-hydroxy-[1,4'-bipiperidine]-1'-carboxylate

https://huagongshe.com/reaction/1060806

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Piperidin-4-olHCID 79341—
반응물tert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매TetrahydrofuranHCID 8028—
생성물tert-Butyl 4-hydroxy-[1,4'-bipiperidine]-1'-carboxylateHCID 9835508—

반응 단계

To 1-tert-butoxycarbonyl-4-piperidone (200 g, 1.01 mol) in tetrahydrofuran (THF) (1500 ml) was added 4-hydroxypiperidine (78.1 g, 0.77 mol). The resultant slurry was stirred for 30 minutes before cooling the reaction mixture with ice/water, acetic acid (47 ml) is then added (exotherm) which caused precipitation. The slurry was allowed to warm to room temperature before the addition of sodium triacetoxyborohydride (236 g, 1.12 mol) which was washed in with THF (500 ml). The resultant slurry was stirred overnight at room temperature. To the reaction mixture was added water (2000 ml) to give a solution. The solution was then extracted with diethyl ether (3×1800 ml). The aqueous phase was basified with 10% aq NaOH (950 ml) and extracted with dichloromethane (DCM) (3×1500 ml). The combined DCM layers are dried (MgSO4), filtered and the solvent removed to give the sub-titled compound as a yellow viscous oil, (177 g, 81%; MS: (M+H) 285).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06525070B2
출처 데이터셋uspto-grants-2003_02
ORD IDord-1aabaee4f8a14456bc000454b077cc4b
출처 메모uspto-grants-2003_02