돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1266994생성일: 2026년 10월 27일

p-Bromochlorobenzene → 3-(4-Chlorophenyl)-8-methyl-8-azabicyclo[3.2.1]octan-3-ol

https://huagongshe.com/reaction/1266994

반응식

참여 물질

역할이름HCID투입량
반응물p-BromochlorobenzeneHCID 7806—
반응물Npc164516HCID 79038—
반응물ButyllithiumHCID 178418339—
용매Diethyl EtherHCID 3283—
생성물3-(4-Chlorophenyl)-8-methyl-8-azabicyclo[3.2.1]octan-3-olHCID 43448876%

반응 단계

2.5 M n-butyl lithium (17.96 mL, 40.90 mmol) was added to -70 ° C diethyl ether (35 mL) and 4-bromochlorobenzene (9.03 g, 47.15 mmol) in diethyl ether (20mL) was added dropwise over 20 minutes. The mixture was stirred in the cold for 20 minutes then 8-Methyl-8-aza-bicyclo[3.2.1]octan-3-one (5 g, 35.92 mmol) in diethyl ether (12 mL) was added dropwise over 5 minutes. Cooling bath was removed and when internal temperature of −20° C. was reached the solution was quenched with 1N hydrochloric acid (200 mL). The aqueous layer was raised to pH=10 with ammonium hydroxide and extracted with diethyl ether (three times, 200 mL each). The combined organic layers were washed with brine (100 mL), dried with magnesium sulfate and concentrated to yield racemic3-(4-Chloro-phenyl)-8-methyl-8-aza-bicyclo[3.2.1]octan-3-ol (6.87 g, contains 9% 8-Methyl-8-aza-bicyclo[3.2.1]octan-3-one) as a white solid. Solid was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06552015B2
출처 데이터셋uspto-grants-2003_04
ORD IDord-a5cf765acacb4ff29ab2a4397ecdaa8f
출처 메모uspto-grants-2003_04