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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441569Generated: October 26, 2026

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

https://huagongshe.com/reaction/441569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiocyanic acid, chloromethyl esterHCID 76755—
ReactantSodium MethoxideHCID 10942334—
Reactant3,4,5-Trichloro-N,N-dimethyl-2-sulfanylbenzene-1-sulfonamideHCID 21419291—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
Product3,4,5-Trichloro-N,N-dimethyl-2-((thiocyanomethyl)thio)benzenesulfonamideHCID 21419293—

Reaction Conditions

Temperature62 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04041073
Source datasetuspto-grants-1977_08
ORD IDord-3b97b691c47449878dd058448992cd9d
Source noteuspto-grants-1977_08