Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetophenone | HCID 7410 | — |
| Reactant | 4-Pyridinecarboxaldehyde | HCID 13389 | — |
| Catalyst | Cobalt diacetate | HCID 6277 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 53916417 | HCID 53916417 | — |
Reaction Steps
Pyridine (0.6 g, 7.5 mmol) and Cobalt (ii) acetate (1.3 g, 7.5 mmol) were dissolved in DMF to produce a blue solution of the complex to which was added 4-pyridine carboxaldehyde (5 g, 46.7 mmol) and acetophenone (6.2 g, 51.4 mmol). The resulting mixture was stirred for 18 hours at 90° C. Most of the DMF was evaporated in vacuo and the residue was purified by flash chromatography (silica gel) with 30% EtoAc/Hexane to afford the titled compound, white solid (5 g). ESP+ (Mass Spec) m/z 210 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06774127B2 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-c8064a4380ae44b19a5b312f44cabdd0 |
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| Source note | uspto-grants-2004_08 |
|---|