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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598107Generated: October 31, 2026

Methane → HCID 58938610, compound

https://huagongshe.com/reaction/598107

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantHydrochloric AcidHCID 313—
ReactantPropanalHCID 527—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 86613888HCID 86613888—
CatalystPalladium hydroxideHCID 9942167—
Solvent1,2-DichloroethaneHCID 11—
SolventEthanolHCID 702—
ProductHCID 58938610HCID 5893861043.8%

Reaction Conditions

Temperature40 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897607B2
Source datasetuspto-grants-2011_03
ORD IDord-1405864542a34fd3bbac78fbebfdf548
Source noteuspto-grants-2011_03