反応式
[C:1]1([CH2:7][CH2:8][C:9](Cl)=[O:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Cl:12][C:13]1[CH:18]=[CH:17][C:16]([Mg]Br)=[CH:15][CH:14]=1.[Cl-].[NH4+]>C1C=CC=CC=1.[Cl-].[Cd+2].[Cl-]>[C:1]1([CH2:7][CH2:8][C:9]([C:16]2[CH:17]=[CH:18][C:13]([Cl:12])=[CH:14][CH:15]=2)=[O:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1参加物
6
実験手順
Phenylpropionyl chloride (33.7 g) in benzene was added dropwise to a stirred mixture of 4-chlorophenyl magnesium bromide (derived from 38 g of 4-chlorobromobenzene) and cadmium chloride (37 g) in benzene at 0°. The mixture was stirred at room temperature for 6 hours and aqueous ammonium chloride solution then added. Ether extraction yielded p-chlorophenyl phenylethyl ketone (25 g) m.p. 78°-79°.
後処理
- extractionEther extraction
出典と根拠
- ORDレコード
- ord-61dbe1b7ada641c0b901f2e585d9aef7
- 出典データセット
- uspto-grants-1985_05
- 特許番号
- US04520007
関連ノート
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