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HRID 603336作成日:2026年10月27日

Hydrochloric Acid → N-(4-Ethylphenyl)-2,3,5,6-tetrafluoroaniline

https://huagongshe.com/reaction/603336

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2,3,5,6-TetrafluoroanilineHCID 12786—
反応物1-Bromo-4-ethylbenzeneHCID 15313—
反応物Tris(1,1-dimethylethyl)phosphineHCID 83681—
反応物Sodium t-butoxideHCID 23676156—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物N-(4-Ethylphenyl)-2,3,5,6-tetrafluoroanilineHCID 21938675—

反応条件

温度85 °C

反応手順

A mixture of 2,3,5,6-tetrafluoroaniline (4.5 g, 27.3 mmol), 4-ethylbromobenzene (5.0 g, 27 mmol), toluene (50 ml), sodium tert-butoxide (4.67 g, 48 mmol), tri-tert-butylphosphin (217 mg, 1.07 mmol) and bis-dibenzylideneacetone-palladium(0) (260 mg, 0.45 mmol) is heated under nitrogen to 85° C. for 15.5 h. The mixture is cooled to room temperature and water (30 ml), concentrated hydrochloric acid (20 ml) and hyflo are added. After stirring for 45 minutes, the mixture is filtered and the organic phase is washed with water three times. The solvent is evaporated in vacuo and the residue is chromatographed on silica using hexane/toluene (9:1 to 3:1) affording N-(2′,3′,5′,6′-tetrafluorophenyl)-4-ethylanilin as a liquid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07906677B2
出典データセットuspto-grants-2011_03
ORD IDord-db7c28842a0549feb90e747c0c7962f1
出典メモuspto-grants-2011_03