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HRID 6899作成日:2026年10月24日

Hydrochloric Acid → 2-(3,4-Dichlorophenoxy)-5-fluoro-benzoic acid

https://huagongshe.com/ja/reaction/6899

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3,4-DichlorophenolHCID 7258—
反応物Cesium carbonateHCID 10796—
反応物5-Fluoro-2-iodobenzoic acidHCID 13158583—
触媒copper(II) trifluoromethanesulfonateHCID 2734996—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物2-(3,4-Dichlorophenoxy)-5-fluoro-benzoic acidHCID 22019277—

反応手順

Under N2 in a round-bottomed flask fitted with a reflux condenser and magnetic stirrer were placed 6.37 g (19.55 mmol) of cesium carbonate and 3.2 g (19.55 mmol) of 3,4-dichlorophenol (both from Aldrich Chem. Co., Milwaukee, Wis.) in 60 mL of anhydrous toluene. After stirring the mixture for 5 min., 89 mg (0.24 mmol) of copper (II) trifluoromethanesulfonate (copper triflate) and 0.26g (9.78 mmol) of 5-fluoro-2-iodobenzoic acid (prepared according to the method in Collection of Czechoslovakian Chemical Communications, 1975, vol. 40, p728) were added and the mixture was heated to reflux overnight. Progress of the reaction was monitored using thin layer chromatography (tic), eluting with CHCl3:CH3OH:AcOH (9:1:0.5). After allowing the reaction to cool to room temperature, the mixture was diluted with water and EtOAc; the aqueous layer was acidified with 6 N HCl and re-extracted with additional EtOAc. The organic layers were combined, washed with H2O and saturated NaCl and dried over MgSO4. Removal of the solvent in vacuo gave a dark brown colored oil, 2.6 g, as a mixture of title product and unreacted 5-fluoro-2-iodobenzoic acid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084165B2
出典データセットuspto-grants-2006_08
ORD IDord-fa247d297f624cf2b98f0abe5ea5ce3a
出典メモuspto-grants-2006_08