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HRID 437492作成日:2026年10月26日

Pinacol → 3-[2-Chloro-4-(trifluoromethyl)phenoxy]benzoic acid

https://huagongshe.com/reaction/437492

反応式

関与物質

役割名称HCID仕込み量
反応物PinacolHCID 6425—
反応物3-Hydroxybenzoic AcidHCID 7420—
反応物3,4-DichlorobenzotrifluorideHCID 9481—
反応物Potassium CarbonateHCID 11430—
溶媒Dimethyl SulfoxideHCID 679—
生成物3-[2-Chloro-4-(trifluoromethyl)phenoxy]benzoic acidHCID 91685—

反応手順

To a 300 ml, 3-necked flask equipped with a condenser, stirrer, drying tube and thermometer is charged dimethylsulfoxide (100 ml), anhydrous potassium carbonate (30 g. >0.20 mole), 3,4-dichlorobenzotrifluoride (21.5 g., 0.10 mole), pinacol (10 g.) and 3-hydroxybenzoic acid (13.8 g., 0.10 mole). The reaction temperature is then taken slowly to 140°-5° C. while stirring vigorously and maintained as such for 4 days. The reaction mixture is then cooled to room temperature and the inorganic solids removed by filtration prior to pouring the filtrate into water (1200 ml). The aqueous solution is then triturated with CCl4 (2 × 200 ml), decanted and then acidified to pH1 (conc. HCl) to give a tan colored solid, 25,6 g., mp 114°-17° C. This solid is further purified by dissolving in CCl4 (500 ml) and drying with anhydrous MgSO4. The CCl4 solution is reduced in vacuo to give 19.6 g. (62%) of a yellow solid, mp 116°-19° C. Recrystallization of the yellow solid from hexane gives a tan colored solid, 3-(2-chloro-4-trifluoromethylphenoxy)-benzoic acid, mp 122°-3° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04031131
出典データセットuspto-grants-1977_06
ORD IDord-ade202437c154813abd7b04ebec10f85
出典メモuspto-grants-1977_06