Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389578Generated: November 3, 2026

Propargyl bromide → HCID 178459972, compound

https://huagongshe.com/reaction/1389578

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantSodium hydrideHCID 24758—
ReactantHCID 21263165HCID 21263165—
ReactantHCID 178526276HCID 178526276—
ProductHCID 178459972HCID 178459972—

Reaction Steps

1.31 g. of sodium hydride (55% strength suspension) are added to a solution of 6.15 g. of 2-[(2,6-dichlorophenyl)imino]-1-hydroxyimidazolidine in 45 ml. of absolute dimenthylformamide at a temperature of 25°. After 30 minutes, 4.16 g. of propargyl bromide are added dropwise. After 30 minutes, the mixture is poured onto 500 ml. of a saturated solution of sodium chloride and the aqueous phase is extracted with ether. The ether extracts are washed with aqueous hydrochloric acid. The aqueous extracts are then rendered basic with 3 N caustic soda solution and extracted with ether. After evaporating off the solvent, the residue is dissolved in ether, and hydrogen chloride in dioxane is added. The residue is recrystallized from methanol/acetonitrile, whereupon 2-[(2,6-dichlorophenyl)imino]-1-(2-propynyloxy)-imidazolidine hydrochloride, m.p. 198°-199° (from methanol/acetonitrile) is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04244957
Source datasetuspto-grants-1981_01
ORD IDord-dc8bf9ede1714beca937ecd00520cb2f
Source noteuspto-grants-1981_01