HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 20380010, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Azacyclonol | HCID 15723 | — |
| Reactant | 4-Chlorobutyrophenone | HCID 253533 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 20380010 | HCID 20380010 | — |
Reaction Steps
To 53.4 g (0.2 mole) of α,α -diphenyl-4-piperidinemethanol in 1 liter of toluene was added 38.4 g (0.21 mole) of 4-chlorobutyrophenone, 21 g (0.25 mole) of sodium bicarbonate and 0.1 g of potassium iodide. The mixture was stirred and refluxed for 72 hours then filtered. The filtrate was concentrated to 300 ml and allowed to stand at room temperature until a precipitate formed. The precipitate was filtered off and dissolved in hot toluene, filtered and cooled. A solid formed which was dissolved in diethyl ether and treated with ethereal HCl. The resulting product was recrystallized from methanolbutanone to give the title compound, M.P. 193.5°-195° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03965257 |
| Source dataset | uspto-grants-1976_06 |
| ORD ID | ord-5ae62002dc8543cca5f16b8c22602571 |
| Source note | uspto-grants-1976_06 |