反応式
[C:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10](=O)[CH3:11])=[CH:6][CH:5]=1)(=O)[CH3:2].[C:13]1([OH:19])[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>>[CH3:2][C:1]([C:16]1[CH:17]=[CH:18][C:13]([OH:19])=[CH:14][CH:15]=1)([C:16]1[CH:17]=[CH:18][C:13]([OH:19])=[CH:14][CH:15]=1)[C:4]1[CH:9]=[CH:8][C:7]([C:10]([CH3:11])([C:16]2[CH:17]=[CH:18][C:13]([OH:19])=[CH:14][CH:15]=2)[C:16]2[CH:17]=[CH:18][C:13]([OH:19])=[CH:14][CH:15]=2)=[CH:6][CH:5]=1参加物
実験手順
0.0215 mols of α,α′-dimethyl-α,α,α′,α′-tetrakis(4-hydroxyphenyl)-p-xylene (produced from 1,4-diacetylbenzene and phenol and having a melting point of 307° C.), 9.2 mols of bisphenol A, 9.4 liters of an aqueous solution of 2.0 N sodium hydroxide, and 8 liters of dichloromethane were put into a 50 liters container equipped with a stirrer, and stirred therein, to which phosgene was introduced for 30 minutes. Next, 0.44 mols of bisphenol A, 0.022mols of triethylamine, and 4.5 liters of an aqueous solution of 0.2 N sodium hydroxide were added thereto, and reacted for 40 minutes, and thereafter the aqueous phase and the organic phase in the reaction mixture were separated from each other. Thus was prepared a dichloromethane solution of an oligocarbonate.
出典と根拠
- ORDレコード
- ord-af0f685bc8e84499939123ce07ee12b0
- 出典データセット
- uspto-grants-2001_04
- 特許番号
- US06222004B1
関連ノート
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