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HRID 2358866作成日:2026年10月25日

Hydrochloric Acid → N-(1,1-Dimethyl-2-methylthioethyl)-N'-[2-methyl-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl]phthalamide

https://huagongshe.com/reaction/2358866

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Methyl chloroformateHCID 6586—
反応物Phthalic AnhydrideHCID 6811—
反応物Sodium BicarbonateHCID 516892—
反応物4-(1,1,1,2,3,3,3-Heptafluoropropan-2-yl)-2-methylanilineHCID 9925543—
反応物N-[1,1-dimethyl-2-(methylthio)ethyl]phthalamic acidHCID 11437082—
反応物2-Propanamine, 2-methyl-1-(methylthio)-HCID 12097380—
溶媒1,2-DichloroethaneHCID 11—
溶媒TriethylamineHCID 8471—
生成物N-(1,1-Dimethyl-2-methylthioethyl)-N'-[2-methyl-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl]phthalamideHCID 2206622692%

反応手順

A mixture of 2-methyl-1-methylthio-2-propanamine (11.61 g) and triethylamine (1.97 g) was added dropwise to a mixture of phthalic anhydride (14.42 g) and 1,2-dichloroethane (58 mL) at 50° C. The resulting mixture was stirred at the same temperature for 30 minutes to prepare N-[1,1-dimethyl-2-(methylthio)ethyl]phthalamic acid. Aqueous sodium hydrogencarbonate solution (9.81 g/101 mL) was added dropwise to this mixture at 40° C. and then methyl chloroformate (11.04 g) was added dropwise thereto at the same temperature. After completion of the dropwise addition, the reaction mixture was stirred at 50° C. for 1 hour and the organic layer was separated to prepare a solution of N-[1,1-dimethyl-2-(methylthio)ethyl]isophthalimide in 1,2-dichloroethane. This solution was added dropwise to a mixture of 2-methyl-4-[1,2,2,2-tetrafluoro-1-(trifluoro-methyl)ethyl]aniline (25.45 g), concentrated hydrochloric acid (0.49 g) and 1,2-dichloroethane (14.4 mL) at 60° C., and then stirred at 65° C. for 30 minutes. The reaction mixture was cooled and then neutralized with an aqueous sodium hydrogencarbonate solution, after which the organic layer was separated. The organic layer obtained was concentrated under reduced pressure, and the crystals precipitated were filtered, washed with water and then dried to obtain 47.06 g (yield 92%) of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07763750B2
出典データセットuspto-grants-2010_07
ORD IDord-6524f59788c141b3b9e38fde66526570
出典メモuspto-grants-2010_07