HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl-(2-piperidin-2-yl-ethyl)-amine → 1-(9-Xanthenyl)-2-(2-dimethylaminoethyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl-(2-piperidin-2-yl-ethyl)-amine | HCID 296295 | — |
| Reactant | 9-Acetoxyxanthene | HCID 12543454 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 1-(9-Xanthenyl)-2-(2-dimethylaminoethyl)piperidine | HCID 21512550 | — |
Reaction Steps
A solution of 3.12 g. (0.02 mole) of 2-(2-dimethylaminoethyl)piperidine and 4.8 g. (0.02 mole) of 9-acetoxyxanthene in 75 ml. of anhydrous benzene was refluxed for 20 hours. The cooled solution was washed with 100 ml. of a 5 percent aqueous sodium bicarbonate solution, dried over anhydrous potassium carbonate, filtered, and evaporated in vacuo. The residue was taken up in low boiling petroleum ether and filtered to remove dixanthenyl ether. The filtrate was chromatographed on 125 g. of alumina, eluting successively with petroleum ether, petroleum etherbenzene mixtures, benzene, and finally ether. Evaporation of the ether fractions gave 1-(9-xanthenyl)-2-(2-dimethylaminoethyl)piperidine, m.p. 64°-67°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03980788 |
| Source dataset | uspto-grants-1976_09 |
| ORD ID | ord-613d4b6d8ccd46bf882576d6fb7b57c2 |
| Source note | uspto-grants-1976_09 |