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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371576Generated: October 27, 2026

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

https://huagongshe.com/reaction/371576

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantDiallylcarbamyl chlorideHCID 3449313—
ReactantHCID 178477666HCID 178477666—
SolventTriethylamineHCID 8471—
Product1-Diallylcarbamoyl-3-ethylsulphonyl-1,2,4-triazoleHCID 20355134—

Reaction Steps

A mixture of 6.45 g. 3-ethylsulphonyl-1,2,4-triazole, 6.6 g. diallylcarbamoyl chloride, 25 ml. dry tetrahydrofuran and 8 ml. dry triethylamine was refluxed under anhydrous conditions for 1.5 hours. The cooled reaction mixture was filtered and the filtrate distilled under reduced pressure to remove solvent and give a product which distilled at 187° C./0.2 mm. This product solidified and was recrystallized from petroleum ether (b.p. 60° - 80° C.) to give 1-diallylcarbamoyl-3-ethylsulphonyl-1,2,4-triazole, m.p. 39° - 42° C. Elemental analysis satisfactory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04087269
Source datasetuspto-grants-1978_05
ORD IDord-b034d7629ba14ffa9a5cf825914d638a
Source noteuspto-grants-1978_05