Methane → HCID 69135034、化合物

HRID 969510ノート

反応式

HRID 969510 の反応式
[C:1]([N:4]([C:8]1[C:13]([N+:14]([O-])=O)=[CH:12][C:11]([Br:17])=[CH:10][C:9]=1[O:18][CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)C(=O)C)(=[O:3])[CH3:2].C.O.NN>CO.[Fe](Cl)(Cl)Cl>[NH2:14][C:13]1[CH:12]=[C:11]([Br:17])[CH:10]=[C:9]([O:18][CH2:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[C:8]=1[NH:4][C:1](=[O:3])[CH3:2]

参加物

6

実験手順

A suspension of 23 g (56 mmol) N-acetyl-N-(2-benzyloxy4-bromo-6-nitro-phenyl)-acetamide, 5.5 g (34 mmol) iron(III) chloride and 13.8 g activated charcoal in 600 ml methanol was heated to reflux. To the reaction mixture were added 28 ml hydrazine hydrate (95%) to maintain gentie reflux. After complete reaction (2 h), the reaction mixture was cooled down and filtered through celite. The filter cake was washed thoroughly with dichloromethane/methanol and the filtrate was evaporated to dryness. The residue was partitioned between dichloromethane/methanol and water. The organic layer was washed with brine, dried over anhydrous magnesium sulphate and evaporated. The residue was recrystallized from boiling ethyl acetate/n-heptane to give 12.3 g (65%) of the title compound as a colourless solid. m.p. 185° C.

後処理

  1. temperaturewas heated to reflux
  2. temperatureto maintain gentie
  3. temperaturereflux
  4. customAfter complete reaction (2 h)
  5. temperaturethe reaction mixture was cooled down
  6. filtrationfiltered through celite
  7. washThe filter cake was washed thoroughly with dichloromethane/methanol
  8. customthe filtrate was evaporated to dryness
  9. customThe residue was partitioned between dichloromethane/methanol and water
  10. washThe organic layer was washed with brine
  11. dry with materialdried over anhydrous magnesium sulphate
  12. customevaporated
  13. customThe residue was recrystallized

出典と根拠

ORDレコード
ord-a39b2eb00b114f41ad10364a6d830536
出典データセット
uspto-grants-2007_12
特許番号
US07307084B2

反応ノート

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