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 the solution was separated with 20% aqueous sodium hydroxide solution. After the ether layer was dried with 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 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 | US04549023 |
| Source dataset | uspto-grants-1985_10 |
| ORD ID | ord-5fcc18ac3029427fbd0a24db0cd7705f |
| Source note | uspto-grants-1985_10 |