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HRID 2350951作成日:2026年10月26日

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

https://huagongshe.com/reaction/2350951

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物2,4-Dichloro-m-toluidineHCID 88282—
反応物2-Methyl-1,5-diphenylpentane-1,3,5-trioneHCID 14303545—
溶媒ChlorobenzeneHCID 7964—
生成物2,4-dichloro-3-methylphenyl-3-methyl-2,6-diphenyl-4(1H)-pyridinoneHCID 14303688—

反応手順

In 170 ml of chlorobenzene were dissolved 3.4 g (0.012 mole) of 2-methyl-1,5-diphenyl-1,3,5-pentanetrione and 10.6 g (0.06 mole) of 2,4-dichloro-3-methylaniline, followed by further addition of 4.1 g (0.022 mole) of para-toluenesulfonic acid and 35.0 g of Molecular Sieves 5A to the solution. After heating the reaction mixture under reflux for 2 hours, solid matter was removed from the reaction mixture, followed by an addition of 200 ml of chloroform. The resultant mixture was washed first with 100 ml of 10% hydrochloric acid and then with 100 ml of a 10% aqueous solution of sodium hydroxide. The mixture was washed further with water and was then dried over anhydrous sodium sulfate. Subsequent to removal of the sodium sulfate, the solvent was distilled off and the residue was purified by chromatography on a silica gel column (eluent: ethyl acetate). Upon recrystallization of the resultant crystals from a 2:1 mixed solvent of acetone and hexane, 0.7 g of 1-(2,4-dichloro-3-methylphenyl)-3-methyl-2,6-diphenyl-4(1H)-pyridinone having a melting point of 237°-238° C. was obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04871751
出典データセットuspto-grants-1989_10
ORD IDord-92581976988c440ea0569d9240c742fd
出典メモuspto-grants-1989_10