反応式
Cl[C:2]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)([CH3:4])[CH3:3].[Cl-].[Al+3].[Cl-].[Cl-].C(=O)([O-])[O-].[K+].[K+].[CH:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>>[C:21]1([C:2]([C:5]2[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=2)([CH3:4])[CH3:3])[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1参加物
5
実験手順
541 g of 2-chloro-2-phenylpropane (3.5 mol) were added dropwise at 5° C. with stirring to a suspension of 35 g of clean pulverised aluminium chloride in 3.5 1 of dry benzene in the course of 5 h, and the mixture was kept at 5° C. for a further 15 min. and then poured onto ice. The benzene phase was neutralised with potassium carbonate after separating off the aqueous phase, dried and freed from excess benzene. 650 g of crude product were obtained, which was fractionally distilled through a column about 100 cm long. 527 g (78% of the theoretical yield) of 2,2-diphenylpropane passed over at 152°-160° C. and 20 mbar.
後処理
- additionpoured onto ice
- customafter separating off the aqueous phase
- customdried
- custom650 g of crude product were obtained
- distillationwhich was fractionally distilled through a column about 100 cm long
出典と根拠
- ORDレコード
- ord-193197b993104ef3819548ba8c81bd21
- 出典データセット
- uspto-grants-1993_02
- 特許番号
- US05185467
関連ノート
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