2-azido-1-(4-bromophenyl)ethanone → 2-Amino-1-(4-bromophenyl)ethanone
反応式
[N:1]([CH2:4][C:5]([C:7]1[CH:12]=[CH:11][C:10]([Br:13])=[CH:9][CH:8]=1)=[O:6])=[N+]=[N-]>CO.[Pd]>[NH2:1][CH2:4][C:5]([C:7]1[CH:12]=[CH:11][C:10]([Br:13])=[CH:9][CH:8]=1)=[O:6]参加物
4
実験手順
To a solution of compound 2-azido 4′-bromoacetophenone (1.0 g, 4.17 mmol) in MeOH (20 mL), Pd/C (10%, 100 mg) was added to the solution. The mixture was degassed and stirred under hydrogen system for 4 hours. The mixture was filtered and evaporated in vacuo without further purification to obtain 2-amino 4′-bromoacetophenone (0.535 g, 2.499 mmol, 60% yield). 1H NMR (d-MeOH) 4.63 (d, J=4.8 Hz, 2H), 7.62 (d, J=7.2 Hz, 2H), 8.03 (d, J=7.2 Hz, 2H) ppm.
後処理
- customThe mixture was degassed
- filtrationThe mixture was filtered
- customevaporated in vacuo without further purification
出典と根拠
- ORDレコード
- ord-a439926c934c441b97dea3795376fc73
- 出典データセット
- uspto-grants-2013_03
- 特許番号
- US08394742B2
反応ノート
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