HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → N-Benzylidene(piperidin-4-yl)methanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | 4-(Aminomethyl)piperidine | HCID 23527 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-Benzylidene(piperidin-4-yl)methanamine | HCID 11820173 | 100% |
Reaction Steps
Benzaldehyde (28.0 g; 0.264 mol) was added, dropwise, to a solution of 4-aminomethylpiperidine (30.2 g; 0.264 mol) in toluene (100 ml). The solution thus obtained was kept stirred at room temperature. After 3 h, the solvent was removed by evaporation at reduced pressure and the residue was taken up twice in toluene. 53.4 g of N-hexahydro-4-pyridinylmethyl-N-phenylmethylidenamine was thus obtained, and was used in subsequent reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08507528B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-f286687ca0bc48c695fc6fd5ade1f076 |
| Source note | uspto-grants-2013_08 |