HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Amino-1-methylpiperidine → N-(N-methyl-4-piperidinyl)-9-xanthenylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Amino-1-methylpiperidine | HCID 2737531 | — |
| Reactant | 9-Acetoxyxanthene | HCID 12543454 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | N-(N-methyl-4-piperidinyl)-9-xanthenylamine | HCID 21482845 | — |
Reaction Steps
A solution of 4.0 g. of 9-acetoxyxanthene and 1.9 g. of 4-amino-1-methylpiperidine in 100 ml. of dry benzene was refluxed for 24 hours. The cooled solution was then washed with 5% aqueous sodium carbonate solution and the organic layer was dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The residue crystallized on triturating with hexane and was recrystallized from hexane to give N-(N-methyl-4-piperidinyl)-9-xanthenylamine, m.p. 96.5°-98° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04005208 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-24ab40c942164b57ba21fc04a8375798 |
| Source note | uspto-grants-1977_01 |