HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenylpiperazine → 1-Phenoxy-4-(4-phenyl-1-piperazinyl)-2-butanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Chloro1-phenoxy-2-butanol | HCID 13120342 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 1-Phenoxy-4-(4-phenyl-1-piperazinyl)-2-butanol | HCID 14422903 | — |
Reaction Steps
A mixture of 6.5 g (0.04 mole) of 1-phenylpiperazine, 8.4 g (0.042 mole) of 4-chloro-1-phenoxy-2-butanol and 15.9 g (0.15 mole) of anhydrous sodium carbonate in 200 ml of 1-butanol was heated at reflux 20 hr. The mixture was concentrated under reduced pressure and the residue was partitioned between water and benzene. The benzene layer was washed with water and aqueous saturated sodium chloride solution, dried over sodium sulfate and concentrated under reduced pressure to give the title product in the residue which was recrystallized from isopropyl alcohol to give 8.9 g (68%) of white powder, m.p. 93°-94° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04806555 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-303220ce004d4fad8b1340743f36b87e |
| Source note | uspto-grants-1989_02 |