HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → N-benzylpiperidine-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | 4-Piperidinecarboxamide | HCID 3772 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-benzylpiperidine-4-carboxamide | HCID 3868064 | 51.7% |
Reaction Steps
To a suspension of isonipecotamide (12.3 g, 96 mmol) in 200 mL of dichloromethane, was added, benzaldehyde (10.6 g, 100 mmol) and sodium triacetoxyborohydride (29.7 gm, 140 mmol) and the mixture was stirred at room temperature for 5 days. The thick white mixture was diluted with 100 mL water and extracted with EtOAc (2×20 mL) The aqueous phase was basified with 1N NaOH to pH 22 12. The resulting white precipitate was collected by suction filtration. The white solid was subsequently taken up in 50 mL of EtOAc, and was washed with 20 mL of brine, then dried (MgSO4), filtered and concentrated to give 10.84 g (50%) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07608618B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-9f6ced7b52864182937ca60b840dfc01 |
| Source note | uspto-grants-2009_10 |