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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796736Generated: October 26, 2026

Tetrahydrofuran → 3-[4-(3,3-Diphenyl-1-propyl)piperazin-1-yl]benzoic acid

https://huagongshe.com/reaction/1796736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 3-[4-(3,3-diphenyl-1-propyl)piperazin-1-yl]benzoateHCID 22180549—
SolventMethanolHCID 887—
Product3-[4-(3,3-Diphenyl-1-propyl)piperazin-1-yl]benzoic acidHCID 2218048785.6%

Reaction Conditions

Temperature65 °C

Reaction Steps

The compound (2.00 g) prepared in step (b) was dissolved in a mixed solvent composed of tetrahydrofuran (20 ml) and methanol (10 ml), and a 1 mol/l aqueous sodium hydroxide solution (10 ml) was added to the solution. The mixture was then stirred at 65° C. for one hr. The solvent was removed from the reaction solution by distillation under the reduced pressure. Water (30 ml) was then added to the residue, and the mixture was adjusted to pH 4 by the addition of 1 mol/l hydrochloric acid. The resultant precipitate was collected by filtration, and was then dried to give 1.60 g (85.6%) of 3-[4-(3,3-diphenyl-1-propyl)piperazin-1-yl]benzoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07030120B2
Source datasetuspto-grants-2006_04
ORD IDord-5ad28e1e4c184bc4a7fbe526ccc40118
Source noteuspto-grants-2006_04