HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → HCID 15895338, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Phenoxypiperidine | HCID 18878 | — |
| Reactant | 1-(3-Bromopropoxy)-4-fluorobenzene | HCID 260004 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 15895338 | HCID 15895338 | — |
Reaction Steps
A mixture of 4-phenoxypyridine and benzylbromide in acetone was stirred overnight at room temperature. After removal of the solvent, the residue was dissolved in methanol, cooled to -20° C. and treated portionwise with sodium borohydride, and warmed to 0° C. After a standard workup and purification, the resulting tetrahydropyridine adduct was dissolved in methanol and hydrogenated using 20% Pd-C as a catalyst to provide 4-phenoxypiperidine. A mixture of 4-phenoxypiperidine and 1-bromo-3-(4-fluorophenoxy)propane in acetone with excess potassium carbonate was heated at reflux for 12 hours to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06124323 |
| Source dataset | uspto-grants-2000_09 |
| ORD ID | ord-31ad0bdc912a49ec9a5f4fb96d7d83c5 |
| Source note | uspto-grants-2000_09 |