HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 1-(1-Methyl-3-phenoxypropyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 4-Phenoxy-2-butyl tosylate | HCID 13326762 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(1-Methyl-3-phenoxypropyl)piperidine | HCID 20135812 | 75% |
Reaction Steps
In a sealed tube, 10 g of the 4-phenoxy-2-butyl tosylate was reacted with 11.2 g of piperidine in 60 ml of absolute methyl alcohol for one hour at 125° C. After the reaction solution was condensed under reduced pressure, 100 ml of diethyl ether was added into the solution, and then the solution was separated into the diethyl ether solution and 20% aqueous sodium hydroxide solution. After the ether layer was dried over anhydrous sodium sulfate, ether was removed under reduced pressure therefrom. The residue thus obtained was subjected to an alumina-column chromatography using chloroform as the developing solvent to give 5.46 g of 1-(1-methyl-3-phenoxypropyl)piperidine in a yield of 75%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04751302 |
| Source dataset | uspto-grants-1988_06 |
| ORD ID | ord-2a034c9c197e4a1eb6236f87902bda01 |
| Source note | uspto-grants-1988_06 |