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

HRID 1278973
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인쇄 미리보기

반응식

HRID 1278973 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 g (40.9 mmol) 3-(1-benzylpiperidin-4-yloxy)-propionitrile are dissolved in 100 ml ethanol and added to a spatula tip Raney-Nickel. The mixture is stirred at RT and under hydrogen atmosphere until the consumption of the theoretical amount of hydrogen to be taken up (ca. two days). Subsequently, this is filtered from the catalyst and the solvent is removed under vacuum. The residue is distilled in a bulb tube apparatus. Yield of a colorless oil: 7.5 g (73%).

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후처리

  1. custom(ca. two days)
  2. filtrationSubsequently, this is filtered from the catalyst
  3. customthe solvent is removed under vacuum
  4. distillationThe residue is distilled in a bulb tube apparatus

출처 및 근거

ORD 기록
ord-8da270c868434afa8ec7cdf45c2721af
출처 데이터셋
uspto-grants-2002_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06444823B1

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