HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 4-Phenyl-3-(4-pyridyl)-3-butene-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 4-Pyridinylacetone | HCID 80552 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 4-Phenyl-3-(4-pyridyl)-3-butene-2-one | HCID 53885222 | 78.7% |
Reaction Steps
Using the procedure of Example A-1, step 1, 4-pyridylacetone (step 1) (1 g, 7.4 mmol) was condensed with benzaldehyde (790 mg, 7.4 mmol) in benzene (15 mL) containing piperidine (50 mg) at reflux. The desired 4-phenyl-3-(4-pyridyl)-3-butene-2-one (1.3 g, 78%) was obtained as a crystalline solid: m.p. 101-103° C. Anal. Calc'd for C15H13NO (223.28): C, 80.69; H, 5.87; N, 6.27. Found: C, 80.59; H, 5.79; N, 6.18.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06514977B1 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-c2b32157ec474a3bba33b0abae3f0802 |
| Source note | uspto-grants-2003_02 |