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Ethanol → Ethyl 3-methylpiperidine-4-carboxylate hydrochloride

HRID 525476
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HRID 525476 반응식
Cl.[CH3:2][CH:3]1[CH:8]([C:9]([OH:11])=[O:10])[CH2:7][CH2:6][NH:5][CH2:4]1.O=S(Cl)[Cl:14].[CH3:16][CH2:17]O>>[ClH:14].[CH3:2][CH:3]1[CH:8]([C:9]([O:11][CH2:16][CH3:17])=[O:10])[CH2:7][CH2:6][NH:5][CH2:4]1
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참가 물질

4

반응물 3

HCID 702EthanolHCID 24386Thionyl ChlorideHCID 691690773-Methylpiperidine-4-carboxylic acid hydrochloride

생성물 1

HCID 51358495Ethyl 3-methylpiperidine-4-carboxylate hydrochloride

실험 절차

The mixture of 3-methylpiperidine-4-carboxylic acid hydrochloride (3.3 g, 18.4 mmol, 1.0 eq) and SOCl2 (6.6 g, 55.3 mmol, 3.0 equiv) in EtOH (30 mL) was stirred at reflux for 3 h, and then the reaction mixture was concentrated by vacuum to give compound ethyl 3-methylpiperidine-4-carboxylate hydrochloride as a yellow oil which was used for next step. ESI-MS (M+H)+: 172.2.

후처리

  1. temperatureat reflux for 3 h
  2. concentrationthe reaction mixture was concentrated by vacuum

출처 및 근거

ORD 기록
ord-ab828ab4f8de435cbeaf92e3a367de83
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09340527B2

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