反応式
[Cl:1]Cl.[F:3][C:4]([F:14])([F:13])[O:5][C:6]1[CH:11]=[CH:10][C:9]([OH:12])=[CH:8][CH:7]=1>C(Cl)(Cl)(Cl)Cl>[Cl:1][C:8]1[CH:7]=[C:6]([O:5][C:4]([F:13])([F:14])[F:3])[CH:11]=[CH:10][C:9]=1[OH:12]参加物
4
実験手順
Gaseous chlorine was slowly introduced to a stirred solution of 35.6 g of 4-trifluoromethoxyphenol in 100 ml carbon tetrachloride. The reaction temperature was kept at 20° to 30° C. by outer cooling. After saturaring with chlorine, the reaction mixture was stirred at 20° to 30° C. for 1 hour, cooled, washed with water, dried over anhydrous sodium sulfate, and evaporated to give a pale yellow residue. The residue was distilled under reduced pressure to give 29.8 g of 2-chloro-4-trifluoromethoxyphenol which boiled at 67°-70° C./18 mmHg.
後処理
- customwas kept at 20° to 30° C. by outer cooling
- temperaturecooled
- washwashed with water
- dry with materialdried over anhydrous sodium sulfate
- customevaporated
- customto give a pale yellow residue
- distillationThe residue was distilled under reduced pressure
出典と根拠
- ORDレコード
- ord-e29a4776f309479c9773dc81cfc33bef
- 出典データセット
- uspto-grants-1986_09
- 特許番号
- US04609669
関連ノート
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