Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Propanal | HCID 527 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 86613888 | HCID 86613888 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 58938610 | HCID 58938610 | 43.8% |
Reaction Steps
Ethyl 1-cyano-6-mesityl-4-oxo-4H-quinolizine-3-carboxylate (0.110 g, 0.30 mmol) was dissolved in 20 mL ethanol and HCl (0.15 mL) and treated with 20% Pd(OH)2 over charcoal (0.050 g). The solution was evacuated and filled with a hydrogen balloon. After 5 h, the solution was filtered and concentrated to give a yellow solid. The hydrochloride salt was then dissolved in 1,2-dichloroethane (5 mL) and propionaldehyde (0.078 mL, 1.1 mmol) was added followed by sodium triacetoxyborohydride (0.23 g, 1.1 mmol). The reaction was heated to 40° C. overnight. The solution was cooled, quenched with water. Extraction with ethyl acetate was followed by drying the organic layer, concentration, and flash chromatography (ethyl acetate) to give 0.059 g (42% yield) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07897607B2 |
|---|
| Source dataset | uspto-grants-2011_03 |
|---|
| ORD ID | ord-1405864542a34fd3bbac78fbebfdf548 |
|---|
| Source note | uspto-grants-2011_03 |
|---|