Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885864Generated: October 30, 2026

Potassium Hydroxide → HCID 67049536, compound

https://huagongshe.com/reaction/885864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant2-Propenoic acid, 3-(4-formylphenyl)-HCID 98077—
Reactant1-[4-(4-Acetylphenyl)piperazin-1-yl]ethan-1-oneHCID 23118295—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 67049536HCID 67049536—

Reaction Steps

A mixture of 1-[4-(4-acetyl-piperazin-1-yl)-phenyl]-ethanone (prepared following the procedure described in Example 16 STEP A, 533 mg, 2.16 mmol), 4-formylcinnamic acid (381 mg, 2.16 mmol) and 1.7 M KOH (2.54 ml) in EtOH (15 ml) and water (3 ml) was stirred overnight at room temperature. The resulting precipitate was filtered to get 260 mg of (E)-3-(4-{(E)-3-[4-(4-acetyl-piperazin-1-yl)-phenyl]-3-oxo-propenyl}-phenyl)-acrylic acid as its potassium salt. The mother liquors were acidified with 10% HCl and the resulting green precipitate was filtered to give 240 mg of (E)-3-(4-{(E)-3-[4-(4-acetyl-piperazin-1-yl)-phenyl]-3-oxo-propenyl}-phenyl)-acrylic acid hydrochloride. The mixture of both, the potassium salt and of the hydrochloric salt, was used in the next step without any further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242175B2
Source datasetuspto-grants-2012_08
ORD IDord-6ba3f06eb9cf476a969fdd6aef0126a8
Source noteuspto-grants-2012_08