HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(3-Pyridylmethyl)Pyrrolidine → 3-(Pyrrolidin-1-ylmethyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(3-Pyridylmethyl)Pyrrolidine | HCID 67786 | — |
| Catalyst | Adams' catalyst | HCID 345198 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-(Pyrrolidin-1-ylmethyl)piperidine | HCID 4341894 | — |
Reaction Steps
The educt 3-(1-pyrrolidinylmethyl)-pyridine (24.6 g) is taken up in 250 ml glacial acetic acid and hydrogenated with 2 g of PtO2 under 3 bar H2 at ambient temperature. The solution filtered off is evaporated down, combined with ice and made alkaline with solid KOH while cooling. Afer extracting three times with 250 ml of diethylether the crude product is dried with MgSO4. After the MgSO4 has been filtered off the solvent is eliminated and the amine is distillled in a water jet vacuum at a boiling point of 123° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07709480B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-11e6ccb43d0f4476898481a52cec11e6 |
| Source note | uspto-grants-2010_05 |