反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]=[C:9]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH2:10]C)=[CH:4][CH:3]=1.[Cl-].[Al+3].[Cl-].[Cl-].[C:22]1([C:28]#[C:29][C:30]([O:32]CC)=O)[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1.S(=O)(=O)(O)O.[C:40]1(C)C=CC=CC=1>>[F:1][C:2]1[CH:3]=[CH:4][C:5]([N:8]2[C:9]([C:12]3[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=3)=[CH:10][C:30](=[O:32])[C:29]([CH3:40])=[C:28]2[C:22]2[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=2)=[CH:6][CH:7]=1参加物
実験手順
To 300 ml of toluene were added 9.1 g (0.040 mole) of N-(4fluorophenyl)-1-phenylpropaneimine, 4.7 g (0.035 mole) of aluminum chloride and 5.2 g (0.030 mole) of ethyl phenylpropiolate, followed by refluxing the resultant mixture for 5 hours. Thereafter, the reaction mixture was poured into 500 ml of 2N sulfuric acid which had been ice-cooled, followed by extraction with chloroform. After washing the organic layer with water, the organic layer wad dried over anhydrous sodium sulfate. Subsequent to removal of the sodium sulfate, the solvent was distilled off and the residue was purified by chromatography on a silica gel column (eluent: 1:50 mixed solvent of methanol and chloroform). The resultant crystals were recrystallized from 1:1 mixed solvent of acetone and hexane to give 1.0 g of 1-(4-fluorophenyl)-3-methyl-2,6-diphenyl-4(1H)-pyridinone having a melting point of 256°-259° C.
後処理
- temperaturecooled
- extractionfollowed by extraction with chloroform
- washAfter washing the organic layer with water
- dry with materialthe organic layer wad dried over anhydrous sodium sulfate
- customSubsequent to removal of the sodium sulfate
- distillationthe solvent was distilled off
- customthe residue was purified by chromatography on a silica gel column (eluent: 1:50 mixed solvent of methanol and chloroform)
- customThe resultant crystals were recrystallized from 1:1 mixed solvent of acetone and hexane
出典と根拠
- ORDレコード
- ord-dfd91291af1243c0a38ec9e6f2463d95
- 出典データセット
- uspto-grants-1989_10
- 特許番号
- US04871751
関連ノート
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