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Thionyl Chloride → Ethyl 4-(3-chloro-3-oxopropyl)-1-piperidinecarboxylate

HRID 981619
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인쇄 미리보기

반응식

HRID 981619 반응식
[CH2:1]([O:3][C:4]([N:6]1[CH2:11][CH2:10][CH:9]([CH2:12][CH2:13][C:14]([OH:16])=O)[CH2:8][CH2:7]1)=[O:5])[CH3:2].S(Cl)([Cl:19])=O>ClC(Cl)Cl>[Cl:19][C:14](=[O:16])[CH2:13][CH2:12][CH:9]1[CH2:10][CH2:11][N:6]([C:4]([O:3][CH2:1][CH3:2])=[O:5])[CH2:7][CH2:8]1
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참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 149891953-(1-(Ethoxycarbonyl)piperidin-4-yl)propanoic acid

생성물 1

HCID 14989196Ethyl 4-(3-chloro-3-oxopropyl)-1-piperidinecarboxylate수율 47%

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

To a stirred mixture of 200 parts of 1-(ethoxycarbonyl)-4-piperidinepropanoic acid and 750 parts of trichloromethane were added 320 parts of thionyl chloride. The whole was stirred for 18 hours at room temperature. The reaction mixture was evaporated with methylbenzene. The residue was distilled, yielding 102.6 parts (47%) of ethyl 4-(3-chloro-3-oxopropyl)-1-piperidinecarboxylate; bp. 165-170 at 399 Pa (int. 45).

후처리

  1. customThe reaction mixture was evaporated with methylbenzene
  2. distillationThe residue was distilled

출처 및 근거

ORD 기록
ord-4ef05e2268014532bda894b397d622e2
출처 데이터셋
uspto-grants-1991_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04992433

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