反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([NH:9][C:10]2[CH:15]=[CH:14][C:13]([O:16][CH3:17])=[CH:12][CH:11]=2)=[CH:5][CH:4]=1.[OH2:18].[C:19]1(C)[CH:24]=[CH:23][C:22](S(O)(=O)=O)=[CH:21][CH:20]=1.[F:30][C:31]([F:44])([F:43])[CH2:32][O:33][C:34]1[CH:39]=[CH:38][C:37]([CH2:40][CH:41]=O)=[CH:36][CH:35]=1>C1(C)C=CC=CC=1>[F:30][C:31]([F:44])([F:43])[CH2:32][O:33][C:34]1[CH:39]=[CH:38][C:37]([C:40]([C:19]2[CH:20]=[CH:21][C:22]([O:18][CH2:32][C:31]([F:44])([F:43])[F:30])=[CH:23][CH:24]=2)=[CH:41][N:9]([C:6]2[CH:5]=[CH:4][C:3]([O:2][CH3:1])=[CH:8][CH:7]=2)[C:10]2[CH:15]=[CH:14][C:13]([O:16][CH3:17])=[CH:12][CH:11]=2)=[CH:36][CH:35]=1参加物
実験手順
Using a 30-ml flask similar to that used in Production Example 1, 0.65 g (2.84 mmole) of 4.4'-dimethoxydiphenylamine and 5 mg of p-toluenesulfonic acid monohydrate were added to 10 ml anhydrous toluene solution containing 1.11 g (2.84 mmole) of 1,1-bis(p-2,2,2-trifluoroethoxyphenylacetaldehyde under a nitrogen atmosphere, and refluxed for 3 hours while dehydrating using molecular sieves 4A. After cooling to room temperature, the solution was filtered and the solvent was distilled off. The residue was purified using an alumina column (toluene). The resulting white solid was recrystallized from hexane to yield white crystals of 1,1-bis(p-2,2,2-trifluoroethoxyphenyl)-2-[N,N-bis-(4-methoxyphenyl)amino]ethylene [Compound (4)] in an amount of 1.46 g (yield 85%).
後処理
- temperaturerefluxed for 3 hours
- filtrationthe solution was filtered
- distillationthe solvent was distilled off
- customThe residue was purified
- customThe resulting white solid was recrystallized from hexane
出典と根拠
- ORDレコード
- ord-03bf23159666400c9536128491479c88
- 出典データセット
- uspto-grants-1993_12
- 特許番号
- US05272030
関連ノート
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