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HRID 533494作成日:2026年10月25日

Toluene → Methylthioxanthone

https://huagongshe.com/reaction/533494

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物2-MethylthioxanthoneHCID 27479—
反応物2-Hydroxydithiobenzoic acidHCID 68243—
反応物3-MethylthioxanthoneHCID 375103—
溶媒WaterHCID 962—
溶媒Sulfuric AcidHCID 1118—
生成物MethylthioxanthoneHCID 15566316—

反応条件

温度25 °C

反応手順

Dithiosalicylic acid [product of Wako Pure Chemical Industries, Ltd.] (10 parts) was dissolved in sulfuric acid (139 parts), and the solution was stirred at room temperature (about 25° C.) for one hour and then cooled in an ice bath. Toluene (25 parts) was added dropwise in small portions to the cooled solution, while the temperature of the cooled solution was controlled to 20° C. or lower. Thereafter, the temperature was recovered to room temperature (about 25° C.), and the solution was further stirred for two hours. The resulting reaction mixture was added in small portions to water (815 parts), and precipitated yellow solids were filtered. The yellow solids were dissolved in dichloromethane (260 parts). To the resulting solution, water (150 parts) was added, and then 24% KOH aqueous solution (6.7 parts) was added to alkalinize the aqueous phase. After stirring the resulting mixture for one hour, the aqueous phase was removed by a separation operation, and the organic phase was washed with water (130 parts) three times. Then, the organic phase was dried over anhydrous sodium sulfate, and the organic solvent was evaporated under reduced pressure. As a result, 8.7 parts of an intermediate (C122-2-1) was obtained (as yellow solids). The intermediate (C122-2-1) was a mixture of 2-methylthioxanthone and 3-methylthioxanthone.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08853290B2
出典データセットuspto-grants-2014_10
ORD IDord-2deb2de5dc784fb18db824102e097e46
出典メモuspto-grants-2014_10