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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371569Generated: October 30, 2026

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

https://huagongshe.com/reaction/371569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantDiallylcarbamyl chlorideHCID 3449313—
Reactant3-Butylsulphonyl-1,2,4-triazoleHCID 178455595—
SolventTriethylamineHCID 8471—
Product1-Diallylcarbamoyl-3-butylsulphonyl-1,2,4-triazoleHCID 20354976—

Reaction Steps

A mixture of 5.7 g. 3-butylsulphonyl-1,2,4-triazole, 5.3 g. diallylcarbamoyl chloride, 25 ml. dry tetrahydrofuran and 6 ml. dry triethylamine was refluxed under anhydrous conditions for 1.5 hours. The reaction mixture was worked up as described in Example 1 to give 1-diallylcarbamoyl-3-butylsulphonyl-1,2,4-triazole as an oil which was heated under reduced pressure (100° C./0.5 mm.) for 30 minutes to remove all traces of volatile material. Refractive index of product nD26 1.5132. Elemental analysis satisfactory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04087269
Source datasetuspto-grants-1978_05
ORD IDord-5b1d710ba0bc49a789e9ed4311dc6d58
Source noteuspto-grants-1978_05