HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 4-[4-(1-Methyl-2-naphthalenyloxy)-1-piperidyl]-1-(4-fluorophenyl)-1-butanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 3-(4-Fluorobenzoyl)propyl chloride | HCID 19750 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | 4-(1-Methyl-2-naphthalenyloxy)piperidine | HCID 20463209 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-[4-(1-Methyl-2-naphthalenyloxy)-1-piperidyl]-1-(4-fluorophenyl)-1-butanone | HCID 20463232 | — |
Reaction Steps
A solution of 3.47 g of (12.5 mmole) of 4-(1-methyl-2-naphthalenyloxy)piperidine, 2.63 g (13.1 mmole) of 4-chloro-1-(4-fluorophenyl)-1-butanone, 5.2 g (52 mmole) of potassium bicarbonate and a pinch of potassium iodide in 60 ml of toluene is heated at reflux for 80 hours. The mixture is partitioned between toluene and water and the organic phase washed with brine, dried over magnesium sulfate, and concentrated in vacuo to yield 4-[4-(1-methyl-2-naphthalenyloxy)-1-piperidyl]-1-(4-fluorophenyl)-1-butanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04443462 |
| Source dataset | uspto-grants-1984_04 |
| ORD ID | ord-40f9672771934035aac58d8d08440ecf |
| Source note | uspto-grants-1984_04 |