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
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
- washthe ethyl acetate layer is washed
- customdried
- distillationdistilled
- customto remove the solvent
- dissolutionThe resulting oil is dissolved in acetone (500 ml)
- additionis added potassium carbonate (40.8 g)
- temperaturethe mixture is refluxed for 2 hours
- distillationacetone is distilled off
- additionTo the residue is added water
- customthe precipitate is separated by filtration
- washwashed
- customdried
- 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
読み込み中…