HuagongsheHuagongshe Chemistry Print Report · For research reference only
9-Acetoxyxanthene → N-methyl-N-(N-ethyl-3-piperidinyl)-9-xanthenylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 9-Acetoxyxanthene | HCID 12543454 | — |
| Reactant | 1-Ethyl-3-methylaminopiperidine | HCID 21482809 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | N-methyl-N-(N-ethyl-3-piperidinyl)-9-xanthenylamine | HCID 21482827 | — |
Reaction Steps
A solution of 3.7 g. (15.4 mmoles) of 9-acetoxyxanthene and 2.2 g. (15.5 mmoles) of 1-ethyl-3-methylaminopiperidine in 80 ml. of benzene was refluxed under nitrogen for 22.5 hours. It was then cooled to room temperature, washed with aqueous sodium bicarbonate solution, and dried over potassium carbonate. After removal of solvent in vacuo, the residue was dissolved in 25 ml. of petroleum ether and filtered from a small amount of crystals. The filtrate was then concentrated in vacuo and chromatographed on silica gel (ether solvent) to give N-methyl-N-(N-ethyl-3-piperidinyl)-9-xanthenylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04005208 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-db5e2acb19934cfd9b687be4999bda80 |
| Source note | uspto-grants-1977_01 |