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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1112744Generated: November 2, 2026

1-Phenylpiperazine → 1-[5-(3,4-Dimethylphenyl)-furan-2-ylmethyl]-4-phenylpiperazine

https://huagongshe.com/reaction/1112744

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylpiperazineHCID 7096—
Reactant5-(3,4-Dimethylphenyl)furan-2-carbaldehydeHCID 960139—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHydrochloride methanolHCID 21893726—
SolventMethanolHCID 887—
Product1-[5-(3,4-Dimethylphenyl)-furan-2-ylmethyl]-4-phenylpiperazineHCID 22762516—

Reaction Steps

5-(3,4-Dimethylphenyl)-furan-2-carboxaldehyde (4.0g;0.02 mole), prepared by the method of C. S. Davis and G. S. Lougheed J.Het.Chem. 4,153, (1967), was added rapidly to a stirred solution of N-phenylpiperazine (3.2g; 0.02 mole) in methanol (30ml) adjusted to pH 7 (using MeOH/HCl). After 30 minutes a solution of sodium cyanoborohydride (0.48g; 0.0075 mole) in methanol (10ml) was added dropwise and the mixture stirred at room temperature for 2 hours. After removal of the methanol by evaporation, the resultant solid was purified by silica gel chromatography. The fractions containing the desired compound were combined, evaporated and the crystalline solid which formed was recrystallised from 60/80° C. petroleum ether to give the title compound, m.p. 110° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04123529
Source datasetuspto-grants-1978_10
ORD IDord-10bd93d474fe453dabfd23b6c88cdfec
Source noteuspto-grants-1978_10