Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606049Generated: October 29, 2026

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

https://huagongshe.com/reaction/1606049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantDiallylcarbamyl chlorideHCID 3449313—
ReactantHCID 178454955HCID 178454955—
SolventTriethylamineHCID 8471—
Product1-Diallylcarbamoyl-3-n-butylthio-1,2,4-triazoleHCID 20355001—

Reaction Steps

A mixture of 6.3 g. 3-n-butylthio-1,2,4-triazole, 6.8 g. diallylcarbamoyl chloride, 25 ml. tetrahydrofuran and 8 ml. dry triethylamine was refluxed under anhydrous conditions for 4 hours. The reaction mixture was worked up as described in Example1 to produce an oil which was distilled under reduced pressure to give 1-diallylcarbamoyl-3-n-butylthio-1,2,4-triazole, b.p. 157°C./0.6 mm. (95.0% 1-isomer by GLC assay). Elemental analysis satisfactory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03952001
Source datasetuspto-grants-1976_04
ORD IDord-9f905554a1f343859be9ba0e9425ff4e
Source noteuspto-grants-1976_04