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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930456Generated: October 30, 2026

6-Bromo-3-pyridinecarboxaldehyde → 5-Formylpyridine-2-carbonitrile

https://huagongshe.com/reaction/930456

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromo-3-pyridinecarboxaldehydeHCID 11769234—
ReactantHCID 178418546HCID 178418546—
SolventDimethylformamideHCID 6228—
Product5-Formylpyridine-2-carbonitrileHCID 1098626335.4%

Reaction Conditions

Temperature120 °C

Reaction Steps

A suspension of 2-bromo-5-formylpyridine (940 mg, 5.05 mmol) and copper (I) cyanide (233 μL, 7.58 mmol) in DMF (8.4 mL) was stirred at 120° C. for 1.5 hours, cooled to RT, and partitioned between water and EtOAc. The solids were removed from the aqueous layer by filtration, and the filtrate was extracted with ethyl acetate. The combined organic layers were washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated. The crude product was purified by silica-gel chromatography, eluting with a gradient of 40%-60% (40% ethyl acetate in heptane) in heptane, to provide the title compound (236 mg, 1.786 mmol) as white solid. LC/MS (ESI+) m/z=133 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296734B2
Source datasetuspto-grants-2016_03
ORD IDord-9cece4c307d54497bd0605e93604a1f0
Source noteuspto-grants-2016_03