N,N-Dimethylaniline → 3-(4-chlorophenyl)-1H-naphtho[2,1-b][1,4]oxazin-2(3H)-one

HRID 5829

反応式

HRID 5829 の反応式
[NH2:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[CH:4][C:3]=1[OH:12].CN(C)C1C=CC=CC=1.O1CCCC1.Br[CH:28]([C:32]1[CH:37]=[CH:36][C:35]([Cl:38])=[CH:34][CH:33]=1)[C:29](Cl)=[O:30]>C(OCC)(=O)C>[Cl:38][C:35]1[CH:36]=[CH:37][C:32]([CH:28]2[O:12][C:3]3[CH:4]=[CH:5][C:6]4[C:11]([C:2]=3[NH:1][C:29]2=[O:30])=[CH:10][CH:9]=[CH:8][CH:7]=4)=[CH:33][CH:34]=1

参加物

6

実験手順

To a mixture of 1-amino-2-naphthol (9.4 g), N,N-dimethylaniline (17.87 g) and tetrahydrofuran (160 ml) is added dropwise α-bromo-4-chlorophenylacetyl chloride (18.97 g) under ice cooling, and the mixture is stirred for one hour. To the reaction mixture is added ethyl acetate, and the ethyl acetate layer is washed, dried and distilled to remove the solvent. The resulting oil is dissolved in acetone (500 ml) and thereto is added potassium carbonate (40.8 g), and the mixture is refluxed for 2 hours, and acetone is distilled off. To the residue is added water, and the precipitate is separated by filtration, washed, dried and recrystallized from tetrahyrofuran to give 3-(4-chlorophenyl)-1H-naphtho[2,1-b][1,4]oxazin-2(3H)-one (13.29 g, yield 72.8%).

後処理

  1. washthe ethyl acetate layer is washed
  2. customdried
  3. distillationdistilled
  4. customto remove the solvent
  5. dissolutionThe resulting oil is dissolved in acetone (500 ml)
  6. additionis added potassium carbonate (40.8 g)
  7. temperaturethe mixture is refluxed for 2 hours
  8. distillationacetone is distilled off
  9. additionTo the residue is added water
  10. customthe precipitate is separated by filtration
  11. washwashed
  12. customdried
  13. customrecrystallized from tetrahyrofuran

出典と根拠

ORDレコード
ord-d364fc4681ef4cc7a031ee2d8b2fe643
出典データセット
uspto-grants-1993_09
特許番号
US05246929

関連ノート

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