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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 253997생성일: 2026년 10월 25일

tert-Butyl 3-oxo-8-azabicyclo(3.2.1)octane-8-carboxylate → tert-Butyl 3-hydroxy-8-azabicyclo(3.2.1)octane-8-carboxylate

https://huagongshe.com/reaction/253997

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl 3-oxo-8-azabicyclo(3.2.1)octane-8-carboxylateHCID 2794767—
반응물Sodium borohydrideHCID 4311764—
용매EthanolHCID 702—
용매DichloromethaneHCID 6344—
생성물tert-Butyl 3-hydroxy-8-azabicyclo(3.2.1)octane-8-carboxylateHCID 2118772593.6%

반응 단계

3-Oxo-8-aza-bicyclo[3.2.1]octane-8-carboxylic acid, tert-butyl ester (8 g, 35.5 mmol) was dissolved in 100 mL of ethanol. Sodium borohydride (2 g, 53.5 mmol) was added to the solution portionwise at room temperature. After stirring for 3 hours, the reaction was evaporated in vacuo to give clear viscous oil. The oil was dissolved in dichloromethane, washed with water and brine, dried over anhydrous sodium sulfate, filtered, and evaporated to afford 7.55 g of 3-hydroxy-8-aza-bicyclo[3.2.1]octane-8-carboxylic acid, tert-butyl ester as a white crystalline solid; 1H NMR (300 MHz, DMSO-d6): 4.23 (dd, J=2.7, 4.6 Hz, 1H), 4.18-4.06 (m, 2H), 2.17-2.06 (m, 1H), 1.99-1.91 (m, 3H), 1.72-1.50 (m, 5H), 1.47 (s, 9H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07872031B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-60de4d44e5b848b48f128104782e2b53
출처 메모uspto-grants-2011_01