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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1097528생성일: 2026년 10월 25일

Dimethylformamide → 3-(Trifluoromethyl)phenylacetyl chloride

https://huagongshe.com/reaction/1097528

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Oxalyl chlorideHCID 65578—
반응물3-(Trifluoromethyl)benzeneacetic acidHCID 67695—
용매TetrahydrofuranHCID 8028—
생성물3-(Trifluoromethyl)phenylacetyl chlorideHCID 12751636—

반응 단계

[3-(Trifluoromethyl)phenyl]acetic acid (4.1 g, 20.1 mmol) was dissolved in tetrahydrofuran (20 mL), and oxalyl chloride (2.1 mL, 24.5 mmol) and N,N-dimethylformamide (5 μL) were added. The reaction mixture was stirred at room temperature for 1 hr, and the solvent was evaporated under reduced pressure to give [3-(trifluoromethyl)phenyl]acetyl chloride. To a solution of 3-amino-4-fluorophenol (2.43 g, 19.1 mmol) in tetrahydrofuran (20 mL) was added a suspension of sodium hydrogen carbonate (2.41 g, 28.6 mmol) in water (30 mL), and the mixture was vigorously stirred at room temperature. A solution of [3-(trifluoromethyl)phenyl]acetyl chloride produced above in tetrahydrofuran (10 mL) was added dropwise to the mixture, and the mixture was stirred at room temperature for 30 min. Ethyl acetate (100 mL) was added to the reaction mixture to separate the aqueous layer. The organic layer was washed with saturated brine (100 mL), and dried over anhydrous magnesium sulfate. Insoluble material was filtered off, and the obtained solution was purified by silica gel chromatography (eluate: ethyl acetate), and the obtained solution was concentrated under reduced pressure to give the title compound (5.84 g, 98%) as a pale-brown solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08143258B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-8afe35c016864cc68df49ac62a830c48
출처 메모uspto-grants-2012_03