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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1779985생성일: 2026년 10월 26일

Ammonium Chloride → 2',4'-Difluoro-2-methyl-3-(4-cyanophenyl)-propiophenone

https://huagongshe.com/reaction/1779985

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물4-(Bromomethyl)benzonitrileHCID 86996—
반응물2',4'-DifluoropropiophenoneHCID 123586—
반응물Lithium HexamethyldisilazideHCID 2733832—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물2',4'-Difluoro-2-methyl-3-(4-cyanophenyl)-propiophenoneHCID 1904920141%

반응 단계

A 19 g portion of 2,4-difluoropropiophenone was dissolved in 150 ml of tetrahydrofuran. With cooling in a dry ice-acetone bath and spending 20 minutes or more, to this was added dropwise 112 ml of 1N tetrahydrofuran solution of lithium hexamethyl disilazide. After 1 hour of stirring at the same temperature, to this was further added dropwise 50 ml of tetrahydrofuran solution containing 14 g of 4-cyanobenzyl bromide spending 20 minutes or more, followed by overnight stirring at room temperature. The reaction solution was mixed with saturated ammonium chloride aqueous solution, poured into water and then extracted with ethyl acetate. The thus obtained organic layer was washed with water and dried on anhydrous magnesium sulfate. After removing the solvent by evaporation under a reduced pressure, the resulting residue was purified by a silica gel column chromatography (ethyl acetate:n-hexane=1:9) to obtain 13 g of 2',4'-difluoro-2-methyl-3-(4-cyanophenyl)-propiophenone with a yield of 41%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05629332
출처 데이터셋uspto-grants-1997_05
ORD IDord-73408bf7f96f437b8f24efa9a97c032e
출처 메모uspto-grants-1997_05