HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Bromide → 1-Ethyl-4-(3-fluorobenzyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-[(3-Fluorophenyl)methyl]piperidine | HCID 10728141 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-Ethyl-4-(3-fluorobenzyl)piperidine | HCID 70983687 | — |
Reaction Steps
Bromoethane (0.1 mL) was added to a mixture of 4-(3-fluorobenzyl)piperidine (Intermediate 180, 0.259 g) and potassium carbonate (0.204 g) in acetonitrile (10 mL). The mixture was stirred for 20 hours then filtered. The filtrate acidified by addition of few drops of 2M HCl and the solution was passed through a SCX-2 column (10 g). The product was eluted with 2M ammonia in methanol and the residue after evaporation was triturated with diethyl ether. The solid was filtered off and the filtrated was concentrated in vacuo to give 1-ethyl-4-(3-fluorobenzyl)piperidine (0.210 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09290472B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-9831bd9934d44785b9a1154d29da9e4c |
| Source note | uspto-grants-2016_03 |