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HRID 441569作成日:2026年10月26日

Thiocyanic acid, chloromethyl ester → 3,4,5-Trichloro-N,N-dimethyl-2-((thiocyanomethyl)thio)benzenesulfonamide

https://huagongshe.com/reaction/441569

反応式

関与物質

役割名称HCID仕込み量
反応物Thiocyanic acid, chloromethyl esterHCID 76755—
反応物Sodium MethoxideHCID 10942334—
反応物3,4,5-Trichloro-N,N-dimethyl-2-sulfanylbenzene-1-sulfonamideHCID 21419291—
溶媒MethanolHCID 887—
溶媒ChloroformHCID 6212—
生成物3,4,5-Trichloro-N,N-dimethyl-2-((thiocyanomethyl)thio)benzenesulfonamideHCID 21419293—

反応条件

温度62 °C

反応手順

To a stirring mixture of 1.5 grams (0.0047 mole) of 3,4,5-trichloro-N,N-dimethyl-2-(mercapto)benzenesulfonamide in 80 milliliters of methanol at 25° C., was added 0.39 grams of sodium methoxide. The mixture was stirred for 15 minutes and thereafter 1.0 gram (0.009 mole) of chloromethylthiocyanate was added thereto and the mixture stirred at room temperature for 3 hours. At the end of this time period, the reaction mixture was filtered to remove the solids which had precipitated. The filtrate further heated at 62° C. for 2 hours and after cooling, the solvent was reduced in volume by evaporation under reduced pressure. The solids were thereafter removed by filtration. Additional filtrations gave additional solids. The recovered solids were combined and dissolved in chloroform and filtered. The solvent was removed by evaporation under reduced pressure and the solid product which remained was air dried. The 3,4,5-trichloro-N,N-dimethyl-2-(thiocyanomethyl)thio)benzenesulfonamide product was recovered in a yield of 0.7 grams (40 percent of theoretical) and melted at 155°-156° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04041073
出典データセットuspto-grants-1977_08
ORD IDord-3b97b691c47449878dd058448992cd9d
出典メモuspto-grants-1977_08