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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1153960Generated: November 1, 2026

Potassium Iodide → HCID 13369910, compound

https://huagongshe.com/reaction/1153960

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
ReactantBenzene, (3-bromopropoxy)-HCID 68522—
ReactantHCID 20435662HCID 20435662—
ReactantHCID 178437794HCID 178437794—
SolventEthanolHCID 702—
SolventAcetonitrileHCID 6342—
ProductHCID 13369910HCID 1336991022%

Reaction Steps

A mixture of 2-[3-[4-(3-chlorophenyl)-1-piperazinyl]propyl]-5-ethyl-1H-1,2,4-triazol-3(2H)-one (3.86 g., 0.01 mole), 3-phenoxypropyl bromide (2.15 g., 0.01 mole), potassium carbonate (4.15 g., 0.01 mole) and a trace of potassium iodide in 50 ml. of acetonitrile is refluxed for a 65 hr. period. The reaction mixture is filtered, the filtrate concentrated under reduced pressure and residual material taken up in ether and filtered. Solvent is removed and further purification carried out by sequentially converting the free base to the hydrochloride salt and then to the free base which is chromatographically treated employing a silica column with methanol/chloroform eluant. Free base, obtained from the chromatographic separation, is converted to the hydrochloride salt in ethanol employing ethanolic hydrogen chloride to afford 1.17 g., (22% yield) of analytically pure 2-[3-[4-(3-chlorophenyl)-1-piperazinyl]propyl]-5-ethyl-2,4-dihydro-4-(3-phenoxypropyl)-3H-1,2,4-triazol-3-one hydrochloride, m.p. 145°-147° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04487773
Source datasetuspto-grants-1984_12
ORD IDord-7a90eb3792cb405a95f1b8538b72feda
Source noteuspto-grants-1984_12