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Thionyl Chloride → tert-Butyl 4-(Chlorocarbonyl)piperidine-1-carboxylate

HRID 552137
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인쇄 미리보기

반응식

HRID 552137 반응식
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][CH:11]([C:14]([OH:16])=O)[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].S(Cl)([Cl:19])=O>C(Cl)(Cl)Cl>[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][CH:11]([C:14]([Cl:19])=[O:16])[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 3928711-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acid

생성물 1

HCID 21906247tert-Butyl 4-(Chlorocarbonyl)piperidine-1-carboxylate

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

To a stirred solution of piperidine-1,4-dicarboxylic acid mono-tert-butyl ester (1.000 g, 4.00 mmol) in chloroform (15 mL) was added thionyl chloride (3.0 mL, 40.00 mmol). The reaction mixture was left stirring at reflux for 3 days and then concentrated in vacuo. The obtained crude solid, 4-chlorocarbonylpiperidine-1-carboxylic acid tert-butyl ester, was used without further purification.

후처리

  1. waitThe reaction mixture was left
  2. temperatureat reflux for 3 days
  3. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-ab4619c99b0f478f900cf85e670c3e66
출처 데이터셋
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07951805B2

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