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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371588Generated: October 31, 2026

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

https://huagongshe.com/reaction/371588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylcarbamoyl chlorideHCID 6916—
ReactantTetrahydrofuranHCID 8028—
Reactant3-Propylsulphinyl-1,2,4-triazoleHCID 178461002—
SolventTriethylamineHCID 8471—
Product1-Diethylcarbamoyl-3-propylsulphinyl-1,2,4-triazoleHCID 20163371—

Reaction Steps

A mixture of 4.8 g. 3-propylsulphinyl-1,2,4-triazole, 4.48 g. diethylcarbamoyl chloride, 40 ml. dry tetrahydrofuran and 6 ml. dry triethylamine was refluxed under anhydrous conditions for 5 hours. The cooled reaction mixture was filtered to remove triethylamine hydrochloride. The filtrate was diluted with petroleum ether (b.p. 40° - 60° C.), causing the deposition of an oil which gradually solidified. The solid product was collected and recrystallized from a mixture of ether and petroleum ether (b.p. 40° - 60° C.) to give 1-diethylcarbamoyl-3-propylsulphinyl-1,2,4-triazole, m.p. 50.5° - 51.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04087269
Source datasetuspto-grants-1978_05
ORD IDord-fa7958c738b740d6adf0d979da26cedf
Source noteuspto-grants-1978_05