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3-[(1-benzyl-4-piperidyl)oxy]propanenitrile → 200868-41-3

HRID 1294466
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반응식

HRID 1294466 반응식
[CH2:1]([N:8]1[CH2:13][CH2:12][CH:11]([O:14][CH2:15][CH2:16][C:17]#[N:18])[CH2:10][CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H][H]>C(O)C.[Ni]>[CH2:1]([N:8]1[CH2:9][CH2:10][CH:11]([O:14][CH2:15][CH2:16][CH2:17][NH2:18])[CH2:12][CH2:13]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 27945993-[(1-benzyl-4-piperidyl)oxy]propanenitrileHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 18425738200868-41-3

시약·촉매·용매 2

HCID 935Nickel촉매HCID 702Ethanol용매

실험 절차

10.0 g (40.9 mmol) 3-(1-benylpiperidin-4-yloxy)-propionitrile are dissolved in 100 ml ethanol and added to a spatula tip of Raney-Nickel. The mixture is stirred at RT under hydrogen atmosphere until the uptake of the theoretical amount of hydrogen (ca. two days). The mixture is filtered from the catalyst and the solvent is removed under vacuum. The residue is distilled in a bulb tube apparatus. Yield of colorless oil: 7.5 g (73%).

후처리

  1. filtrationThe mixture is filtered from the catalyst
  2. customthe solvent is removed under vacuum
  3. distillationThe residue is distilled in a bulb tube apparatus

출처 및 근거

ORD 기록
ord-8f0bc9ba11564026af81e54f68306f68
출처 데이터셋
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07241745B2

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