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Benzyl Bromide → 1-benzyl-1H-pyrazole-3-carbaldehyde

HRID 413283
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인쇄 미리보기

반응식

HRID 413283 반응식
[CH2:1](Br)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH:9]1[CH:13]=[CH:12][C:11]([CH:14]=[O:15])=[N:10]1.C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[CH2:1]([N:9]1[CH:13]=[CH:12][C:11]([CH:14]=[O:15])=[N:10]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7498Benzyl BromideHCID 11430Potassium CarbonateHCID 122183831H-pyrazole-3-carbaldehyde

생성물 1

HCID 114011991-benzyl-1H-pyrazole-3-carbaldehyde수율 61.9%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a solution of benzyl bromide (0.29 g) in N,N-dimethylformamide (9 ml) was added 1H-pyrazole-3-carboxaldehyde (0.15 g) and potassium carbonate (0.24 g). The mixture was stirred at room temperature for 24 hours, silica gel was added, the solvent removed by evaporation and the crude material purified by chromatography (isohexane:ether, 2:1) to give the product as an oil (0.18 g).

후처리

  1. additionsilica gel was added
  2. customthe solvent removed by evaporation
  3. customthe crude material purified by chromatography (isohexane:ether, 2:1)

출처 및 근거

ORD 기록
ord-6d33378c29d04b489b7fbd4671e4aa97
출처 데이터셋
uspto-grants-2003_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06566376B1

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