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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 227569생성일: 2026년 10월 25일

Hydrochloric Acid → (3S,4S)-methyl 4-(3,4-dichlorophenyl)-1-methylpiperidine-3-carboxylate

https://huagongshe.com/reaction/227569

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물ArecolineHCID 2230—
반응물4-Bromo-1,2-dichlorobenzeneHCID 29013—
반응물MagnesiumHCID 5462224—
용매TolueneHCID 1140—
용매Diethyl EtherHCID 3283—
생성물(3S,4S)-methyl 4-(3,4-dichlorophenyl)-1-methylpiperidine-3-carboxylateHCID 4442917425%
생성물HCID 69593838HCID 6959383810%

반응 조건

온도-40 °C

반응 단계

A stirred suspension of magnesium turnings (3.4 g, 142 mmol) in diethyl ether (20 ml) was added a solution of 1-bromo-3,4-dichlorobenzene (29 g, 130 mmol) in diethyl ether (150 ml). The mixture was heated at reflux for 20 minutes and then cooled at −40° C. A solution of arecoline (10 g, 65 mmol) in toluene (100 ml) was added slowly while keeping the internal temperature between −40° C. and −30° C. The reaction mixture was stirred at −20° C. for 6 hours and then added 4 N HCl (50 ml). The phases were then separated and the aqueous phase was added ammonia (aq) until basic pH and extracted with dichloromethane (4×100 ml), dried with magnesium sulfate and evaporated to an oil. The isomers (1) and (2) were separated by column chromatography (petroleum ether, ether, triethylamine 70:25:5) to give 5.0 g (25%) of (1) (mp. 70-75° C.) and 2.0 g (10%) of (2) (oil).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560562B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-0ffb2c59d59e462282e9e7a31baa14c7
출처 메모uspto-grants-2009_07