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HRID 644458作成日:2026年10月24日

5-Chloro-2-methoxyaniline → 5-Chloro-2-methoxy-beta-[3,5-bis(trifluoromethyl)phenyl]styrene

https://huagongshe.com/ja/reaction/644458

反応式

関与物質

役割名称HCID仕込み量
反応物5-Chloro-2-methoxyanilineHCID 66763—
反応物3,5-Bis(trifluoromethyl)styreneHCID 2773242—
反応物Sodium NitriteHCID 23668193—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
溶媒Tetrafluoroboric acidHCID 28118—
生成物5-Chloro-2-methoxy-beta-[3,5-bis(trifluoromethyl)phenyl]styreneHCID 7654613834.7%

反応条件

温度0 °C

反応手順

A solution of sodium nitrite (57 mg, 0.8 mmol) in water (1 mL) was added to a solution of 2-amino-4-chloroanisole (131 mg, 0.8 mmol) in 48% hydrogen tetrafluoroborate (0.3 mL) under ice cooling and argon atmosphere. After the mixture was stirred at 0° C. for 1 hour, a solution of 3,5-bis(trifluoromethyl)styrene (100 mg, 0.4 mmol) in methanol (3 mL) was added and the mixture was stirred at 50° C. for 1 hour. After the reaction mixture was cooled to room temperature, the residue obtained by evaporation of the solvent under reduced pressure was diluted with ethyl acetate. After the solution was washed successively with 2N hydrochloric acid, water and brine, dried over anhydrous sodium sulfate, the residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=5:1) to give the title compound (52.8 mg, 33.3%) as a white powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07700655B2
出典データセットuspto-grants-2010_04
ORD IDord-84c38d26b4db498692231614c5f962f7
出典メモuspto-grants-2010_04