反応式
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[OH:8].C(=O)([O-])O.[Na+].Br[C:15]1[CH:20]=[C:19]([Cl:21])[CH:18]=[CH:17][C:16]=1[CH2:22][C:23](Cl)=[O:24]>C(OCC)(=O)C.O.C1(C)C=CC=CC=1>[Cl:21][C:19]1[CH:20]=[CH:15][C:16]([CH:22]2[C:23](=[O:24])[NH:1][C:2]3[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=3[O:8]2)=[CH:17][CH:18]=1参加物
実験手順
To a solution of 2-aminophenol (13.5 g) in ethyl acetate (150 ml) is added a solution of sodium hydrogen carbonate (15 g) in water (300 ml), and to the mixture is added dropwise a solution of o-bromo-4-chlorophenylacetyl chloride (32.2 g) in toluene with vigorous stirring under ice cooling. After the mixture is stirred at room temperature for one hour, the solvent in the organic layer is distilled off and the residue is dissolved in acetone. To the solution is added potassium carbonate (20 g), and the mixture is stirred at room temperature overnight. The solvent is distilled off and to the residue is added water. The mixture is extracted with ethyl acetate. The ethyl acetate layer is washed, dried and distilled to remove the solvent, and the residue is recrystallized from ethyl acetate-n-hexane to give 2-(4-chlorophenyl)-3-oxo-3,4-dihyro-2H-1,4-benzoxazine (24.0 g) as crystals. M.p. 180.5°-181.5° C.
後処理
- stirringAfter the mixture is stirred at room temperature for one hour
- distillationthe solvent in the organic layer is distilled off
- dissolutionthe residue is dissolved in acetone
- additionTo the solution is added potassium carbonate (20 g)
- stirringthe mixture is stirred at room temperature overnight
- distillationThe solvent is distilled off and to the residue
- additionis added water
- extractionThe mixture is extracted with ethyl acetate
- washThe ethyl acetate layer is washed
- customdried
- distillationdistilled
- customto remove the solvent
- customthe residue is recrystallized from ethyl acetate-n-hexane
出典と根拠
- ORDレコード
- ord-ffca69bda88f4569b98eca5bd5ca7c45
- 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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