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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 258953생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/258953

반응식

참여 물질

역할이름HCID투입량
반응물Thiocyanic acid, chloromethyl esterHCID 76755—
반응물Sodium MethoxideHCID 10942334—
반응물3,4,5-Trichloro-N,N-dimethyl-2-sulfanylbenzene-1-sulfonamideHCID 21419291—
용매MethanolHCID 887—
용매ChloroformHCID 6212—
생성물3,4,5-Trichloro-N,N-dimethyl-2-((thiocyanomethyl)thio)benzenesulfonamideHCID 21419293—

반응 조건

온도62 °C

반응 단계

To a stirring mixture a 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04035407
출처 데이터셋uspto-grants-1977_07
ORD IDord-026a36c5a88347948937c14bcbe3247e
출처 메모uspto-grants-1977_07