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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606061Generated: November 2, 2026

Tetrahydrofuran → 1-Diallylcarbamoyl-3-n-butylsulphinyl-1,2,4-triazole

https://huagongshe.com/reaction/1606061

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantDiallylcarbamyl chlorideHCID 3449313—
Reactant3-Butylsulphinyl-1,2,4-triazoleHCID 178455554—
SolventTriethylamineHCID 8471—
Product1-Diallylcarbamoyl-3-n-butylsulphinyl-1,2,4-triazoleHCID 20355110—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 5.2 g. 3-butylsulphinyl-1,2,4-triazole, 6.0 g. 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 to remove triethylamine hydrochloride and the filtrate distilled under reduced pressure to remove solvent. Finally the residue was maintained at 100°C./0.5 mm. for 30 minutes in order to remove all traces of volatile material from the product. The product, 1-diallylcarbamoyl-3-n-butylsulphinyl-1,2,4-triazole, was obtained as an oil, nD26 1.5277. Elemental analysis satisfactory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03952001
Source datasetuspto-grants-1976_04
ORD IDord-429090962a8d453b87e9b6a1fbb619c9
Source noteuspto-grants-1976_04