Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 441569생성일: 2026년 10월 26일
Thiocyanic acid, chloromethyl ester → 3,4,5-Trichloro-N,N-dimethyl-2-((thiocyanomethyl)thio)benzenesulfonamide
https://huagongshe.com/reaction/441569
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Thiocyanic acid, chloromethyl ester | HCID 76755 | — |
| 반응물 | Sodium Methoxide | HCID 10942334 | — |
| 반응물 | 3,4,5-Trichloro-N,N-dimethyl-2-sulfanylbenzene-1-sulfonamide | HCID 21419291 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | 3,4,5-Trichloro-N,N-dimethyl-2-((thiocyanomethyl)thio)benzenesulfonamide | HCID 21419293 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04041073 |
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| 출처 데이터셋 | uspto-grants-1977_08 |
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| ORD ID | ord-3b97b691c47449878dd058448992cd9d |
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| 출처 메모 | uspto-grants-1977_08 |
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