HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 1-[4-(4-Hydroxy-4-phenylpiperidino)-2,2-diphenylbutyryl]pyrrolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Phenylpiperidin-4-ol | HCID 96387 | — |
| Reactant | (Tetrahydro-3,3-diphenyl-2-furylidene)pyrrolidinium bromide | HCID 22624492 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Product | 1-[4-(4-Hydroxy-4-phenylpiperidino)-2,2-diphenylbutyryl]pyrrolidine | HCID 18972298 | — |
Reaction Steps
A mixture of 13 parts of 1-(tetrahydro-3,3-diphenyl-2-furylidene) pyrrolidinium bromide, 5.3 parts of 4-phenyl-4-piperidinol 8 parts of sodium carbonate, 0.2 parts of potassium iodide and 200 parts of 4-methyl-2-pentanone is stirred and refluxed for 5 hours with water separator. The reaction mixture is cooled and water is added. The organic layer s separated, washed with diluted sodium hydroxide solution, dried, filtered, and while stirring the filtrate, the product is crystallized. It is filtered off and dried, yielding 1-[4-(4-hydroxy-4-phenylpiperidino)-2,2-diphenylbutyryl]pyrrolidine; m.p. 187.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05811078 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-c1a0f47ff0944c0da969e44555674033 |
| Source note | uspto-grants-1998_09 |