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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | 5-(3,4-Dimethylphenyl)furan-2-carbaldehyde | HCID 960139 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | Hydrochloride methanol | HCID 21893726 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-[5-(3,4-Dimethylphenyl)-furan-2-ylmethyl]-4-phenylpiperazine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04123529 |
|---|
| Source dataset | uspto-grants-1978_10 |
|---|
| ORD ID | ord-10bd93d474fe453dabfd23b6c88cdfec |
|---|
| Source note | uspto-grants-1978_10 |
|---|