2-Ethyl-5-nitropyridine → 6-Ethylpyridin-3-amine
反応式
[CH2:1]([C:3]1[CH:8]=[CH:7][C:6]([N+:9]([O-])=O)=[CH:5][N:4]=1)[CH3:2]>[Pd]>[NH2:9][C:6]1[CH:7]=[CH:8][C:3]([CH2:1][CH3:2])=[N:4][CH:5]=1参加物
3
実験手順
2-Ethyl-5-nitropyridine (16.3 g) was dissolved in IMS (200 ml) and hydrogenated at ambient temperature at 1 atmosphere using 10% palladium charcoal (0.5 g) as the catalyst. The mixture was filtered to remove the catalyst and the filtrate evaporated to give 5-amino-2-ethylpyridine as an oil.
後処理
- filtrationThe mixture was filtered
- customto remove the catalyst
- customthe filtrate evaporated
出典と根拠
- ORDレコード
- ord-f00d5da1b84846e3bc1b2c8879fc7088
- 出典データセット
- uspto-grants-1998_07
- 特許番号
- US05780482
反応ノート
読み込み中…