HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Methylpiperidine → HCID 21154844, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Methylpiperidine | HCID 79081 | — |
| Reactant | HCID 19388019 | HCID 19388019 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 21154844 | HCID 21154844 | — |
Reaction Steps
18.85 g (0.10 mol) of 4-chloro-l-(2-thienyl)butanone are run, over a periodof 30 min, into a solution, maintained at 100° C., of 21.8 g (0.22 mol) of 3-methylpiperidine in 35 ml of toluene, and the mixture is heated to reflux for 2 hours. The reaction medium is diluted with ethyl ether andthe mixture is washed with water. The organic phase is extracted with dilute hydrochloric acid solution which, after alkalinisation with sodium hydroxide, is in turn extracted with ethyl ether. The organic phase is dried over dry sodium sulphate and treated with a solution of hydrogen chloride in isopropanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05446060 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-86773fd17b274149a38ae049fd4e9af4 |
| Source note | uspto-grants-1995_08 |