Nitric Acid → 6-Methyl-1,3-dioxaindan-5-amine

HRID 1251832

反応式

HRID 1251832 の反応式
[CH2:1]1[O:9][C:8]2[CH:7]=[CH:6][C:5]([CH3:10])=[CH:4][C:3]=2[O:2]1.[N+:11]([O-])(O)=O.O>C(O)(=O)C>[CH2:1]1[O:2][C:3]2[CH:4]=[C:5]([CH3:10])[C:6]([NH2:11])=[CH:7][C:8]=2[O:9]1

参加物

5

実験手順

To a solution of (3,4-methylenedioxy)toluene (5 ml) in acetic acid (20 ml) cooled with a cold water bath was added, dropwise, nitric acid (70%, 5 ml). The mixture was stirred for 45 min. To work up, water (100 ml) was added and the resulting yellow precipitate was filtered and washed with water until the aqueous filtrate was colorless. The yellow solid was dissolved in EtOAc (250 ml) and dried (MgSO4), and the solid was filtered off. The filtrate was subjected to catalytic hydrogenation (10% Pd/C, 1 atm) for 12 hours. The reaction mixture was then filtered off the catalyst and the filtrate was concentrated on a rotavap to give (3,4-methylenedioxy)-6-methylaniline as a brownish grey solid (5.49g, 87% yield).

後処理

  1. additionwas added
  2. filtrationthe resulting yellow precipitate was filtered
  3. washwashed with water until the aqueous filtrate
  4. dissolutionThe yellow solid was dissolved in EtOAc (250 ml)
  5. dry with materialdried (MgSO4)
  6. filtrationthe solid was filtered off
  7. waitThe filtrate was subjected to catalytic hydrogenation (10% Pd/C, 1 atm) for 12 hours
  8. filtrationThe reaction mixture was then filtered off the catalyst
  9. concentrationthe filtrate was concentrated on a rotavap

出典と根拠

ORDレコード
ord-1881bd3d2d3c4ffa9ba763922ee1a89f
出典データセット
uspto-grants-2002_01
特許番号
US06342610B2

関連ノート

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