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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 590926생성일: 2026년 10월 25일

Oxalyl chloride → N-(2-bromo-4-(perfluoropropan-2-yl)-6-(trifluoromethyl)phenyl)-4-cyano-2,3-difluorobenzamide

https://huagongshe.com/reaction/590926

반응식

참여 물질

역할이름HCID투입량
반응물Oxalyl chlorideHCID 65578—
반응물2-Bromo-4-(1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl)-6-(trifluoromethyl)benzenamineHCID 58297558—
반응물4-Cyano-2,3-difluorobenzoic acidHCID 59226971—
반응물4-Cyano-2,3-difluorobenzoyl chlorideHCID 86654254—
촉매DimethylformamideHCID 6228—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매1,3-Dimethyl-2-imidazolidinoneHCID 6661—
용매Ethyl AcetateHCID 8857—
생성물N-(2-bromo-4-(perfluoropropan-2-yl)-6-(trifluoromethyl)phenyl)-4-cyano-2,3-difluorobenzamideHCID 8665425327%

반응 단계

To a solution of 0.840 g (4.59 mmol) of 4-cyano-2,3-difluorobenzoic acid in 10 ml of dichloromethane were added one drop of DMF and 0.470 ml (5.51 mmol) of oxalyl chloride, followed by stirring at room temperature for 1 hour. The solvent was evaporated under reduced pressure and the obtained 4-cyano-2,3-difluorobenzoyl chloride was added to a solution of 1.56 g (3.83 mmol) of 2-bromo-4-(perfluoropropan-2-yl)-6-(trifluoromethyl)aniline obtained in 1-2 of Example 1 in 5 ml of DMI, followed by stirring at 130° C. for 5 hours. To the reaction liquid were added water and ethyl acetate, and the organic layer was washed with a saturated aqueous sodium hydrogen carbonate solution and saturated brine, and then dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the obtained residue was purified by silica gel column chromatography (eluent solvent; hexane:ethyl acetate=1:0→10:1) to prepare 0.58 g (yield 27%) of a target compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09237745B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-4f64f82865704069866a569a68536290
출처 메모uspto-grants-2016_01