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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Arecoline | HCID 2230 | — |
| 반응물 | 4-Bromo-1,2-dichlorobenzene | HCID 29013 | — |
| 반응물 | Magnesium | HCID 5462224 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | (3S,4S)-methyl 4-(3,4-dichlorophenyl)-1-methylpiperidine-3-carboxylate | HCID 44429174 | 25% |
| 생성물 | HCID 69593838 | HCID 69593838 | 10% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07560562B2 |
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| 출처 데이터셋 | uspto-grants-2009_07 |
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| ORD ID | ord-0ffb2c59d59e462282e9e7a31baa14c7 |
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| 출처 메모 | uspto-grants-2009_07 |
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