HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(9-Xanthenylidene)piperidine → 4-[4-(9-Xanthenylidene)piperidino]-2-butanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(9-Xanthenylidene)piperidine | HCID 15780516 | — |
| Catalyst | Tribenzylmethyl ammonium hydroxide | HCID 21829752 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methyl vinyl ketone | HCID 6570 | — |
| Product | 4-[4-(9-Xanthenylidene)piperidino]-2-butanone | HCID 20371549 | — |
Reaction Steps
One drop of tribenzylmethyl ammonium hydroxide is added to a solution of 7 g of 4-(9-xanthenylidene)-piperidine in 70 cc of ethanol, 4.38 cc of methylvinylketone are then added dropwise, and stirring is effected at 50° for 4 hours. The reaction mixture is then concentrated by evaporation in a vacuum, the residue is dissolved in chloroform, extraction is effected with water, and after drying over magnesium sulphate, concentration is effected by evaporation. The partially crystalline residue is triturated with ether/petroleum ether 1:1 and recrystallized from ethanol. M.P. of the title compound 111°-112°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04072756 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-20235b3223a44cbda69c7b47faca4260 |
| Source note | uspto-grants-1978_02 |