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3-Nitrobenzaldehyde → HCID 67289282, 화합물

HRID 2045217
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HRID 2045217 반응식
[NH2:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[CH:4][CH:3]=1.[N+:10]([C:13]1[CH:14]=[C:15]([CH:18]=[CH:19][CH:20]=1)[CH:16]=O)([O-:12])=[O:11]>C(O)C>[N+:10]([C:13]1[CH:14]=[C:15]([CH:18]=[CH:19][CH:20]=1)[CH:16]=[N:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[CH:4][CH:3]=1)([O-:12])=[O:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 74493-NitrobenzaldehydeHCID 133964-Aminobenzonitrile

생성물 1

HCID 67289282HCID 67289282, 화합물수율 83.6%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of 4-amino-benzonitrile (11.8 g, 100 mmol) and 3-nitro-benzaldehyde (16.6 g, 110 mmol) in ethanol (100 mL) was prepared. The reaction mixture was heated to reflux for 3 h. Then the reaction mixture cooled to room temperature. The solvent was removed in vacuo and the residue was washed with ether to afford 4-[(3-nitro-benzylidene)-amino]-benzonitrile (21 g, 83%) as a white solid: LC/MS m/e calcd for C14H9N3O2 (M+H)+: 252.25, observed: 252.1.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • customwas prepared
  • temperatureThe reaction mixture was heated
  • temperatureto reflux for 3 h
  • customThe solvent was removed in vacuo
  • washthe residue was washed with ether
  • 출처 및 근거

    ORD 기록
    ord-339cfef6df9047a78a7199f86b0eb732
    출처 데이터셋
    uspto-grants-2013_11
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08586747B2

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