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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606062Generated: November 2, 2026

Tetrahydrofuran → 1-Diallylcarbamoyl-3-ethylsulphinyl-1,2,4-triazole

https://huagongshe.com/reaction/1606062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantDiallylcarbamyl chlorideHCID 3449313—
ReactantHCID 178477619HCID 178477619—
SolventTriethylamineHCID 8471—
Product1-Diallylcarbamoyl-3-ethylsulphinyl-1,2,4-triazoleHCID 20355074—

Reaction Steps

A mixture of 4.35 g. 3-ethylsulphinyl-1,2,4-triazole, 6.0 ml. diallylcarbamoyl chloride, 25 ml. dry tetrahydrofuran and 7.5 ml. dry triethylamine was refluxed under anhydrous conditions for 2 hours. The reaction mixture was filtered and the filtrate distilled under reduced pressure to remove solvent, giving a residual oil which solidified on cooling. This solid product was recrystallized from petroleum ether (b.p. 60° - 80°C.) to give 1-diallylcarbamoyl-3-ethylsulphinyl-1,2,4-triazole, m.p. 41° - 43°C. Elemental analysis satisfactory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03952001
Source datasetuspto-grants-1976_04
ORD IDord-9dbe93f1407e44d085ee78e1fca4a3ce
Source noteuspto-grants-1976_04