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Piperidine → Benzyl 4-(piperidin-1-ylmethylene)piperidine-1-carboxylate

HRID 574881
노트
인쇄 미리보기

반응식

HRID 574881 반응식
[CH:1]([CH:3]1[CH2:8][CH2:7][N:6]([C:9]([O:11][CH2:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)=[O:10])[CH2:5][CH2:4]1)=O.[NH:19]1[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]1>C1(C)C=CC=CC=1>[N:19]1([CH:1]=[C:3]2[CH2:8][CH2:7][N:6]([C:9]([O:11][CH2:12][C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)=[O:10])[CH2:5][CH2:4]2)[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 8082PiperidineHCID 2776272Benzyl 4-formylpiperidine-1-carboxylate

생성물 1

HCID 86642880Benzyl 4-(piperidin-1-ylmethylene)piperidine-1-carboxylate

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

To a solution of benzyl 4-formylpiperidine-1-carboxylate (12.5 g) in toluene (120 mL) was added piperidine (6.46 g). The mixture was stirred at reflux under a Dean-Stark trap overnight. The mixture was then concentrated under vacuum and the residue was used directly in the next step.

후처리

  1. temperatureat reflux under a Dean-Stark trap overnight
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • concentrationThe mixture was then concentrated under vacuum
  • 출처 및 근거

    ORD 기록
    ord-ea304ae74df147febc885a03a5fb81b2
    출처 데이터셋
    uspto-grants-2015_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US09034875B2

    반응 노트

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