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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375533Generated: October 25, 2026

4-Hydroxybenzaldehyde → Benzaldehyde, 4-(3-(4-phenyl-1-piperazinyl)propoxy)-

https://huagongshe.com/reaction/375533

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantSodium hydrideHCID 24758—
ReactantPiperazine, 1-(3-chloropropyl)-4-phenyl-HCID 139197—
SolventDimethylformamideHCID 6228—
ProductBenzaldehyde, 4-(3-(4-phenyl-1-piperazinyl)propoxy)-HCID 5523469.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

Sodium hydride (3.59 g of 60% in oil) is added to 4-hydroxybenzaldehyde (9.95 g) in dimethylformamide (250 mL) and the mixture stirred at 60° C. for 30 minutes. 1-(3-Chloropropyl)-4-phenylpiperazine (Step A) (19.5 g) is added and the mixture stirred for 14 hours at 60° C. The solvent is evaporated and the residue treated with water (300 mL) and extracted with dichloromethane (3×150 mL). The extracts are dried over magnesium sulfate, filtered and evaporated to leave a beige solid. This solid is recrystallized from ethyl acetate/diethyl ether to give 18.4 g of the title compound as a light beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05486517
Source datasetuspto-grants-1996_01
ORD IDord-0498d120f60344b48fdaa4502b8c9272
Source noteuspto-grants-1996_01