HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 21552950, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Azacyclonol | HCID 15723 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | HCID 14268798 | HCID 14268798 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 21552950 | HCID 21552950 | — |
Reaction Steps
A mixture of 32.0 g (0.12 mole) of α,α-diphenyl-4-piperidinemethanol, 38.0 g (0.15 mole) of 4'-tert-butyl-5-chlorovalerophenone, 27.8 g (0.2 mole) of potassium bicarbonate, and 200 mg of potassium iodide in about 500 ml of toluene is stirred and refluxed for 142 hours then filtered while hot. About 50 ml of ether is added to the filtrate which is then made acidic using ethereal HCl. The resulting precipitate is recrystallized from methanol-butanone to give 4'-tert-butyl-5-[4-(α-hydroxy-α-phenylbenzyl)piperidino]valerophenone hydrochloride, M.P. 209.5°-211°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03946022 |
| Source dataset | uspto-grants-1976_03 |
| ORD ID | ord-c9eaa05fda04402aa60c80c9b622c073 |
| Source note | uspto-grants-1976_03 |