HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 20379985, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Azacyclonol | HCID 15723 | — |
| Reactant | 4-Chloro-1-(2-thienyl)butan-1-one | HCID 123511 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 20379985 | HCID 20379985 | — |
Reaction Steps
A mixture of 53.5 g (0.2 moles) of α,α -diphenyl-4-piperidinemethanol, 41.5 g (0.22 mole) of 4-chloro-1-(2-thienyl)-1-butanone, 33.6 g (0.4 mole) of sodium bicarbonate and a small amount of potassium iodide in 1 liter of toluene was refluxed for 24 hours then filtered. The filtrate was cooled to room temperature, treated with charcoal, and filtered. The solvent was removed under vacuum and 500 ml of diethyl ether was added to dissolve the residue, followed by treatment with ethereal HCl. The resulting precipitate was recrystallized from methanolbutanone to give the desired product, M.P. 192.5°-193.5°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03965257 |
| Source dataset | uspto-grants-1976_06 |
| ORD ID | ord-cfbac79bf2cf4ca39a9c9ce27df78759 |
| Source note | uspto-grants-1976_06 |