N-Ethyl-3-nitropyridin-4-amine → 4-N-ethylpyridine-3,4-diamine

HRID 1817148ノート

反応式

HRID 1817148 の反応式
[CH2:1]([NH:3][C:4]1[CH:9]=[CH:8][N:7]=[CH:6][C:5]=1[N+:10]([O-])=O)[CH3:2]>C(O)C.[Pd]>[CH2:1]([NH:3][C:4]1[CH:9]=[CH:8][N:7]=[CH:6][C:5]=1[NH2:10])[CH3:2]

参加物

4

反応物 1

HCID 21937597N-Ethyl-3-nitropyridin-4-amine

生成物 1

HCID 120363924-N-ethylpyridine-3,4-diamine収率 94%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 702Ethanol溶媒

実験手順

Ethyl-(3-nitropyridin-4-yl)amine (8.7 g, 52.0 mmol) in ethanol (150 ml) was hydrogenated for 18 hours in the presence of 10% palladium on carbon. After filtration of the catalyst through celite, the filtrate was concentrated in vacuo to afford the title compound (6.7 g, 94%).

後処理

  1. filtrationAfter filtration of the catalyst through celite
  2. concentrationthe filtrate was concentrated in vacuo

出典と根拠

ORDレコード
ord-deec0302e37a4813932eacecd3306528
出典データセット
uspto-grants-2009_10
特許番号
US07598251B2

反応ノート

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