HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → Ethyl 1-(pyridin-4-yl)piperidine-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl 4-piperidinecarboxylate | HCID 70770 | — |
| Reactant | 4-Chloropyridine hydrochloride | HCID 81852 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | Ethyl 1-(pyridin-4-yl)piperidine-4-carboxylate | HCID 9899468 | — |
Reaction Steps
4.0 g (26.6 mmol) of 4-chloropyridine hydrochloride, 4.2 g (26.6 mmol) of ethyl piperidine-4-carboxylate and 7.4 ml (53.2 mmol) of triethylamine were stirred in 100 ml of xylene at 130° C. for 24 hours. The reaction mixture was treated with dichloromethane as extracting solvent by an ordinary method to obtain the crude compound, which was purified by the silica gel column chromatography to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06784191B2 |
| Source dataset | uspto-grants-2004_08 |
| ORD ID | ord-1c7c10de9df743bfa2f87502d3d30915 |
| Source note | uspto-grants-2004_08 |