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HRID 845298作成日:2026年10月27日

Pentafluoroaniline → 3-methyl-1-(2,3,4,5,6-pentafluorophenyl)-2,6-diphenyl-4(1H)-pyridinone

https://huagongshe.com/reaction/845298

反応式

関与物質

役割名称HCID仕込み量
反応物PentafluoroanilineHCID 13040—
反応物2-Methyl-1,5-diphenylpentane-1,3,5-trioneHCID 14303545—
溶媒O-XyleneHCID 7237—
生成物3-methyl-1-(2,3,4,5,6-pentafluorophenyl)-2,6-diphenyl-4(1H)-pyridinoneHCID 1430369427.7%

反応手順

In 110 ml of xylene were dissolved 3.1 g (0.011 mole) of 2-methyl-1,5-diphenyl-1,3,5-pentanetrione, 20.0 g (0.11 mole) of 2,3,4,5,6-pentafluoroaniline, 3.1 g (0.016 mole) of paratoluenesulfonic acid and 22.0 g of Molecular Sieves 5A, followed by reflux for 1 hours. After cooling the reaction mixture, solid matter was removed by filtration and the filtrate was then concentrated. After 200 ml of chloroform was added, the resultant solution in chloroform was washed first with 50 ml of 10% hydrochloric acid and then with 50 ml of a 10% aqueous solution of sodium hydroxide. After washing the solution in chloroform further with water, it was dried over anhydrous sodium sulfate. Subsequent to removal of the sodium sulfate, the solvent was distilled off and the residue was subjected to column chromatography (eluent: 50:1 mixed solvent of chloroform and methanol). The resulting crystals were recrystallized from a 1:1 mixed solvent of acetone and hexane, thereby affording 1.3 g of 3-methyl-1-(2,3,4,5,6-pentafluorophenyl)-2,6-diphenyl-4(1H)-pyridinone having a melting point of 192°-194° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04757081
出典データセットuspto-grants-1988_07
ORD IDord-4ef7abd484324b428735bd7ac7cba367
出典メモuspto-grants-1988_07