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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 441569Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/441569

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktThiocyanic acid, chloromethyl esterHCID 76755—
EduktSodium MethoxideHCID 10942334—
Edukt3,4,5-Trichloro-N,N-dimethyl-2-sulfanylbenzene-1-sulfonamideHCID 21419291—
LösungsmittelMethanolHCID 887—
LösungsmittelChloroformHCID 6212—
Produkt3,4,5-Trichloro-N,N-dimethyl-2-((thiocyanomethyl)thio)benzenesulfonamideHCID 21419293—

Reaktionsbedingungen

Temperatur62 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04041073
Quelldatensatzuspto-grants-1977_08
ORD IDord-3b97b691c47449878dd058448992cd9d
Quellennotizuspto-grants-1977_08