HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropanol → 1-(o-Chlorophenoxy)-4-(4-phenyl-1-piperazinyl)-2-butanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-(o-Chlorophenoxy)-2-hydroxybutyl chloride | HCID 19840239 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 1-(o-Chlorophenoxy)-4-(4-phenyl-1-piperazinyl)-2-butanol | HCID 13120451 | — |
Reaction Steps
A mixture of 35.1 g (0.15 mole) of 1-(o-chlorophenoxy)-2-hydroxybutyl chloride, 32.6 g (0.2 mole) of N-phenylpiperazine and 400 ml of 2-propanol was heated at reflux for 48 hr. The resulting reaction mixture was allowed to stand in a refrigerator overnight and filtered. The filtrate was treated with ethereal hydrogen chloride and precipitated with ether. Upon filtering, a white crystalline solid formed which was dissolved in dilute hydrochloric acid and the mixture was then neutralized with aqueous sodium hydroxide producing a crystalline precipitate. This was recrystallized with isopropanol yielding 36 g of the free base, m.p. 100°-101.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04882330 |
| Source dataset | uspto-grants-1989_11 |
| ORD ID | ord-633d4877f7c74007851f781356d8dbb4 |
| Source note | uspto-grants-1989_11 |