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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606096Generated: November 1, 2026

Diethylcarbamoyl chloride → 1-Diethylcarbamoyl-3-diallylsulphamoyl-1,2,4-triazole

https://huagongshe.com/reaction/1606096

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylcarbamoyl chlorideHCID 6916—
ReactantTriethylamineHCID 8471—
ReactantHCID 178457344HCID 178457344—
SolventTetrahydrofuranHCID 8028—
Product1-Diethylcarbamoyl-3-diallylsulphamoyl-1,2,4-triazoleHCID 21324268—

Reaction Steps

A mixture of 6.9 g. 3-diallylsulphamoyl-1,2,4-triazole, 4.5 g. diethylcarbamoyl chloride, 6 ml. triethylamine and 25 ml. dry tetrahydrofuran was refluxed under anhydrous conditions for 1.5 hours. The cooled reaction mixture was filtered to remove triethylamine hydrochloride and the filtrate was evaporated to remove solvent. The solid residue was recrystallized from petroleum ether, b.p. 60° - 80°C., to give 1-diethylcarbamoyl-3-diallylsulphamoyl-1,2,4-triazole, m.p. 49° - 51°C. Elemental analysis satisfactory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03952001
Source datasetuspto-grants-1976_04
ORD IDord-7dce2d67e7c045ad84a8765449c8b1b8
Source noteuspto-grants-1976_04