Ethanol → 2-(4-Aminophenyl)acetamide

HRID 641061

反応式

HRID 641061 の反応式
[N+:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)([O-])=O.[NH2:10]N.[CH2:12]([OH:14])[CH3:13]>[Ni]>[NH2:1][C:4]1[CH:9]=[CH:8][C:7]([CH2:13][C:12]([NH2:10])=[O:14])=[CH:6][CH:5]=1

参加物

5

実験手順

To a suspension of Nitrobenzene (NB-2-A13, NB-2-A14 or NB-3-A16; 1.61 mmol) and Raney Ni (50 mg) in refluxing ethanol (10 mL) was added drop-wise anhydrous hydrazine (0.5 mL). After the addition was complete, the mixture was refluxed for an additional 20 minutes and then filtered through a pad of Celite. The Celite bed was washed with ethanol (100 mL) and the combined solution was evaporated under reduced pressure to provide pure 2-(4-aminophenyl)-acetamide (2-NB-2-A13, 2-NB-2-A14 or 2-NB-3-A16).

後処理

  1. additionAfter the addition
  2. temperaturethe mixture was refluxed for an additional 20 minutes
  3. filtrationfiltered through a pad of Celite
  4. washThe Celite bed was washed with ethanol (100 mL)
  5. customthe combined solution was evaporated under reduced pressure

出典と根拠

ORDレコード
ord-bf03270b059c4d4cbdbf83f0b49e3002
出典データセット
uspto-grants-2010_04
特許番号
US07692005B2

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