Acetic Acid → 2-(1H-pyrrol-1-yl)aniline

HRID 429651

反応式

HRID 429651 の反応式
[N:1]1([C:6]2[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=2[N+:12]([O-])=O)[CH:5]=[CH:4][CH:3]=[CH:2]1.C(O)(=O)C>C(O)C.[Fe]>[N:1]1([C:6]2[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=2[NH2:12])[CH:2]=[CH:3][CH:4]=[CH:5]1

参加物

5

反応物 2

HCID 176Acetic AcidHCID 5206111-(2-Nitrophenyl)pyrrole

生成物 1

HCID 801232-(1H-pyrrol-1-yl)aniline収率 92.2%

試薬・触媒・溶媒 2

HCID 23925Iron触媒HCID 702Ethanol溶媒

実験手順

To a solution of 2-(1-pyrrolyl)nitrobenzene (1.11 g) in ethanol (30 ml) were added iron powder (1.65 g) and acetic acid (3.54 g) and the mixture was refluxed for 1 hour. The reaction mixture was filtered through a bed of celite and the filtrate was concentrated in vacuo. The residue was diluted with a mixture of ethyl acetate and saturated aqueous sodium bicarbonate solution and the mixture was filtered through a bed of celite again. The organic layer was separated and washed with water and brine. The solution was dried over sodium sulfate and the solvent was evaporated in vacuo to give 2-(1-pyrrolyl)phenylamine (860 mg).

後処理

  1. temperaturethe mixture was refluxed for 1 hour
  2. filtrationThe reaction mixture was filtered through a bed of celite
  3. concentrationthe filtrate was concentrated in vacuo
  4. additionThe residue was diluted with a mixture of ethyl acetate and saturated aqueous sodium bicarbonate solution
  5. filtrationthe mixture was filtered through a bed of celite again
  6. customThe organic layer was separated
  7. washwashed with water and brine
  8. dry with materialThe solution was dried over sodium sulfate
  9. customthe solvent was evaporated in vacuo

出典と根拠

ORDレコード
ord-1df4deed1d2e4fc6ae64460029a1deab
出典データセット
uspto-grants-2001_11
特許番号
US06316482B1

関連ノート

読み込み中…