HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-(1-Methyl-4-piperidyl)-1-(2-phenyl-4-quinolyl)-ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(2-Phenyl-4-quinolyl)-2-(4-piperidyl)-ethanol | HCID 13075286 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(1-Methyl-4-piperidyl)-1-(2-phenyl-4-quinolyl)-ethanol | HCID 15581674 | 37.9% |
Reaction Steps
A mixture of 2.55 g of 1-(2-phenyl-4-quinolyl)-2-(4-piperidyl)-ethanol (racemic), 1.1 g of methyl iodide and 0.6 g of potassium carbonate in 20 ml of dimethylformamide was stirred for 2 hours at the ambient temperature. 20 ml of water and 30 ml of toluene were then added. The organic phase was separated, wahsed with water, dried over magnesium sulfate and evaporated under reduced pressure. 1 g of crude product was obtained which was fixed on a column of silica gel. The elution was effected with a 9/1 chloroform-diethylamine mixture. 0.57 g of 2-(1-methyl-4-piperidyl)-1-(2-phenyl-4-quinolyl)-ethanol (racemic), which melted at 208° C. was thus isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04613607 |
| Source dataset | uspto-grants-1986_09 |
| ORD ID | ord-3e1c7d050ac640d99fdcd095c742432d |
| Source note | uspto-grants-1986_09 |