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HRID 256090作成日:2026年10月25日

Hydrochloric Acid → 2,6-Dichloro-4-(2,2,2-trifluoroethylthio)-phenol

https://huagongshe.com/reaction/256090

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Potassium CarbonateHCID 11430—
反応物2,2,2-Trifluoroethyl benzenesulfonateHCID 296341—
反応物2,6-Dichloro-4-mercaptophenolHCID 3016363—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物2,6-Dichloro-4-(2,2,2-trifluoroethylthio)-phenolHCID 1367217471.1%

反応手順

64 g of potassium carbonate were added to a solution of 41.9 g of 3,5-dichloro-4hydroxy-benzenethiol in 200 ml of N,N-dimethylformamide under nitrogen atmosphere. To the stirred mixture were dropped at 30° to 40° C. 55 g of 2,2,2-trifluoroethyl-benzenesulfonate. The whole was stirred at 60° to 70° C. for 6 hours, cooled, mixed with 1.5 l of water, and acidified to pH 2 by dropwise addition of hydrochloric acid. A resulted oil was extracted with toluene and the toluene extract was washed with water. The washed toluene extracted was stirred with 160 ml of a 25% aqueous potassium hydroxide solution, and a water layer was separated. Then the separated water layer was acidified to pH 2 by adding hydrochloric acid. A resulted oil was extracted with toluene. The toluene extract was washed with water, dried over anhydrous sodium sulphate, and evaporated to give a residue. The residue was distilled under reduced pressure to give 42.3 g of 2,6 -dichloro-4-(2,2,2-trifluoroethylthio)-phenol which boiled at 85° to 88° C./1 mmHg.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04700006
出典データセットuspto-grants-1987_10
ORD IDord-19b04108669b4a16a152bd3686fd0efc
出典メモuspto-grants-1987_10