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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2350949생성일: 2026년 10월 25일

p-Toluenesulfonic acid → 1-(2,6-difluorophenyl)-3-methyl-2,6-diphenyl-4(1H)-pyridinone

https://huagongshe.com/reaction/2350949

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물2,6-DifluoroanilineHCID 79647—
반응물2-Methyl-1,5-diphenylpentane-1,3,5-trioneHCID 14303545—
용매O-XyleneHCID 7237—
생성물1-(2,6-difluorophenyl)-3-methyl-2,6-diphenyl-4(1H)-pyridinoneHCID 1430364118.7%

반응 단계

To 150 ml of xylene were added 2.8 g (0.010 mole) of 2-methyl-1,5-diphenyl-1,3,5-pentanetrione, 12.9 g (0.010 mole) of 2,6-diflouroaniline, 3.0 g (0.016 mole) of para-toluenesulfonic acid and 30.0 g of Molecular Sieves 5A, followed by refluxing the resulting mixture for 3 hours. After cooling the reaction mixture, solid matter was filtered off and the filtrate was washed successively with 50 ml of 10% hydrochloric acid, 50 ml of 10% aqueous solution of sodium hydroxide and water. The filtrate was then dried over anhydrous sodium sulfate. Subsequent to removal of the sodium sulfate by filtration, the solvent was distilled off and the residue was crystallized from a 2:1 mixed solvent of acetone and hexane to give 0.7 g of 1-(2,6-diflourophenyl)-3-methyl-2,6-diphenyl-4(1H)-pyridinone having a melting point of 219°-221° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04871751
출처 데이터셋uspto-grants-1989_10
ORD IDord-3cca8642282c4cb2a8c22d3b91d2da6b
출처 메모uspto-grants-1989_10