Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606088Generated: November 3, 2026

Triethylamine → HCID 20290177, compound

https://huagongshe.com/reaction/1606088

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDiallylcarbamyl chlorideHCID 3449313—
ReactantHCID 178468149HCID 178468149—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20290177HCID 20290177—

Reaction Steps

A solution of 4.1 g. 3-(2-ethoxyethylsulphonyl)-1,2,4-triazole, 3.5 g. diallylcarbamoyl chloride and 4 ml. triethylamine in 40 ml. dry tetrahydrofuran was refluxed under anhydrous conditions for 15 hours. The cooled reaction mixture was filtered to remove triethylamine hydrochloride and the filtrate was evaporated to remove solvent. The residue was triturated with petroleum ether (b.p. 40° - 60°C.) to give a solid product. This product was collected and recrystallised from ether/petroleum ether b.p. 40° - 60°C. to give 1-diallylcarbamoyl-3-(2-ethoxyethylsulphonyl)-1,2,4-triazole, m.p. 62° - 63°C. Elemental analysis satisfactory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03952001
Source datasetuspto-grants-1976_04
ORD IDord-c3bd3d20cb2041c2ab4788f4683753b0
Source noteuspto-grants-1976_04