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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837714Generated: November 2, 2026

Ammonia → 3-Pyridinecarbonitrile, 5-formyl-6-methoxy-

https://huagongshe.com/reaction/1837714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHydrochloric AcidHCID 313—
ReactantSodium CyanideHCID 8929—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 22678608HCID 22678608—
CatalystHCID 178418397HCID 178418397—
SolventAcetoneHCID 180—
SolventPropionitrileHCID 7854—
Product3-Pyridinecarbonitrile, 5-formyl-6-methoxy-HCID 2267867368.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

2.00 g of 5-bromo-2-methoxy-3-pyridinecarboxaldehyde dimethyl acetal was dissolved in 25 ml of propionitrile. To the mixture were added 449 mg of sodium cyanide, 152 mg of cuprous iodide and 462 mg of tetrakis(triphenylphosphine)palladium, followed by stirring at 100° C. for 45 minutes in nitrogen atmosphere. A diluted ammonia was added to the reaction solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and brine, and then dried over anhydrous magnesium sulfate. The solvent was evaporated, to give an oil. The oil was dissolved in 16 ml of acetone, 4 ml of 5N-hydrochloric acid was added thereto, and the mixture was left for 30 minutes at room temperature. An aqueous sodium carbonate aqueous solution was added to the reaction solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and brine, and then dried over anhydrous magnesium sulfate. The solvent was evaporated, and the crude product was purified by silica gel column chromatography (toluene:ethyl acetate=1:1), to give 843 mg of the title compound as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06784192B2
Source datasetuspto-grants-2004_08
ORD IDord-8971683554db45fd958b06e1be245f9c
Source noteuspto-grants-2004_08