HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482789Generated: October 30, 2026
Potassium Iodide → HCID 13369910, compound
https://huagongshe.com/reaction/482789
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzene, (3-bromopropoxy)- | HCID 68522 | — |
| Reactant | HCID 20435662 | HCID 20435662 | — |
| Reactant | HCID 178437794 | HCID 178437794 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 13369910 | HCID 13369910 | 22% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04575555 |
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| Source dataset | uspto-grants-1986_03 |
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| ORD ID | ord-64f9f42c5536450e80ad2d0974ce542f |
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| Source note | uspto-grants-1986_03 |
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