HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 4-Methoxy-4-methylpiperidine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 3-(4-Fluorobenzoyl)propyl chloride | HCID 19750 | — |
| Reactant | 4-Methoxy-4-methylpiperidine | HCID 20373710 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-Methoxy-4-methylpiperidine hydrochloride | HCID 20373709 | — |
Reaction Steps
A solution of 20.1 g (0.1 m) of gamma-chloro-p-fluorobutyrophenone, 30 g (0.2 m) of 4-methyl-4-methoxy-piperidine and 0.1 g. of potassium iodide in 150 ml of toluene is heated in a glass autoclave for 15 hours at 100°-110° C. The KI and the 4-methyl-4-methoxy-piperidine hydrochloride formed in the reaction are separated by filtration and the solvent removed from the filtrate by evaporation under a vacuum on a steam bath. The obtained base is dissolved in ether and the hydrochloride is precipitated with alcoholic HCl. The reaction product is purified by recrystallization from ethanol-ether. Yield 22 g. Melting point 182° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04070473 |
| Source dataset | uspto-grants-1978_01 |
| ORD ID | ord-4ab173b5d613407d8003c1e5290fd547 |
| Source note | uspto-grants-1978_01 |