HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → Benzamide, N-(1-piperidinylmethyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Benzamide | HCID 2331 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Benzamide, N-(1-piperidinylmethyl)- | HCID 100673 | 893.3% |
Reaction Steps
Benzamide (0.5 g, 0.4 mmol) was dissolved in 5 mL of methanol. To this stirred solution piperidine (0.35 mL, 0.4 mol) was added and the resulting solution was cooled in an ice bath. Formaldehyde (0.31 mL, 0.4 mol, 37% in water) was added dropwise. The solution was stirred for 10 min and then it was refluxed for 4 h. After cooling, the solvents were evaporated to give Mannich base 15 as a white solid 0.78 g (87% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08410075B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-3660bc308f124ea9a926c90fd16e0588 |
| Source note | uspto-grants-2013_04 |