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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497324Generated: November 1, 2026

4-(Naphthalen-1-yl)butanoic acid → HCID 22318647, compound

https://huagongshe.com/reaction/497324

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Naphthalen-1-yl)butanoic acidHCID 13077—
ReactantThionyl ChlorideHCID 24386—
CatalystDimethylformamideHCID 6228—
SolventTolueneHCID 1140—
ProductHCID 22318647HCID 22318647—

Reaction Conditions

Temperature70 °C

Reaction Steps

0.37 g of 4-Naphthalen-1-yl-butyric acid was dissolved in 5.0 ml of toluene, and 0.35 ml of thionyl chloride and 1 drop of dimethylformamide were added, followed by heating at 70° C. for 30 minutes. The reaction solution was cooled to room temperature and concentrated under reduced pressure to give a crude 4-naphthalen-1-yl-butyryl chloride. To the resulting crude 4-naphthalen-1-yl-butyryl chloride was added 2.3 ml of a toluene solution of 0.40 g of 1-[2-(4-fluorophenyl)-2-(4-methylpiperazino)ethyl]piperazine, followed by stirring at room temperature for 30 minutes. To the reaction solution was added a saturated aqueous sodium bicarbonate solution and, after extraction with ethyl acetate, the organic layer was dried over anhydrous sodium sulfate. After removal of the drying agent by filtration, the filtrate was concentrated under reduced pressure, and the residue was purified by a silica gel column chromatography (Wako-gel C-200, chloroform:methanol=10:1) to give 0.58 g of 1-[2-(4-fluorophenyl)-2-(4-methylpiperazino)ethyl]-4-(4-naphthalen-1-yl-butyryl)piperazine as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06949552B2
Source datasetuspto-grants-2005_09
ORD IDord-c90e0be27dc7468098446024b6b4073e
Source noteuspto-grants-2005_09