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HRID 644458생성일: 2026년 10월 24일

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

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

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참여 물질

역할이름HCID투입량
반응물5-Chloro-2-methoxyanilineHCID 66763—
반응물3,5-Bis(trifluoromethyl)styreneHCID 2773242—
반응물Sodium NitriteHCID 23668193—
용매MethanolHCID 887—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
용매Tetrafluoroboric acidHCID 28118—
생성물5-Chloro-2-methoxy-beta-[3,5-bis(trifluoromethyl)phenyl]styreneHCID 7654613834.7%

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07700655B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-84c38d26b4db498692231614c5f962f7
출처 메모uspto-grants-2010_04