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Potassium Carbonate → 5-(1-Benzylpiperidin-4-yl)-1-hydroxyiminopentylamine

HRID 54538
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반응식

HRID 54538 반응식
[CH2:1]([N:8]1[CH2:13][CH2:12][CH:11]([CH2:14][CH2:15][CH2:16][CH2:17][C:18]#[N:19])[CH2:10][CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(=O)([O-])[O-].[K+].[K+].Cl.[NH2:27][OH:28]>>[CH2:1]([N:8]1[CH2:13][CH2:12][CH:11]([CH2:14][CH2:15][CH2:16][CH2:17][C:18]([NH2:19])=[N:27][OH:28])[CH2:10][CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 11430Potassium CarbonateHCID 443297Hydroxyamine hydrochlorideHCID 19959227HCID 19959227, 화합물

생성물 1

HCID 539824105-(1-Benzylpiperidin-4-yl)-1-hydroxyiminopentylamine수율 62.8%

실험 절차

A mixture of 1-benzyl-4-(4-cyanobutyl)piperidine (2.20 g), potassium carbonate (3.56 g) and hydroxylamine hydrochloride (2.39 g) was heated under reflux for 20 hours. After cooling, the mixture was filtered and evaporated in vacuo. The residue was dissolved in ether, filtered and recrystallized to afford 5-(1-benzylpiperidin-4-yl)-1-hydroxyiminopentylamine (1.56 g).

후처리

  1. temperature
was heated
  • temperatureunder reflux for 20 hours
  • temperatureAfter cooling
  • filtrationthe mixture was filtered
  • customevaporated in vacuo
  • dissolutionThe residue was dissolved in ether
  • filtrationfiltered
  • customrecrystallized
  • 출처 및 근거

    ORD 기록
    ord-5d4b3a8d5160406a86c5d92721ee746b
    출처 데이터셋
    uspto-grants-1997_04
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05622976

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