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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371585Generated: October 30, 2026

Tetrahydrofuran → HCID 20354997, compound

https://huagongshe.com/reaction/371585

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantDiallylcarbamyl chlorideHCID 3449313—
ReactantHCID 178455553HCID 178455553—
SolventDichloromethaneHCID 6344—
ProductHCID 20354997HCID 20354997—

Reaction Steps

A mixture of 5.76 g. 3-sec.butylsulphinyl-1,2,4-triazole, 5.31 g. diallylcarbamoyl chloride, 50 ml. dry tetrahydrofuran and 5 ml. dry triethylamine was kept under anhydrous conditions at room temperature for 72 hours. The reaction mixture was filtered and the filtrate evaporated under reduced pressure at room temperature to give a residual oil which was dissolved in methylene dichloride. The resulting solution was washed with water, dried over anhydrous sodium sulphate and distilled under reduced pressure at room temperature to give 1-diallylcarbamoyl-3-sec.butylsulphinyl-1,2,4-triazole as a residual oil, nD25 1.5268, for which a satisfactory elemental analysis was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04087269
Source datasetuspto-grants-1978_05
ORD IDord-7b499f774313477dac3fe81e8ed51225
Source noteuspto-grants-1978_05