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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1526562Generated: November 4, 2026

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

https://huagongshe.com/reaction/1526562

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 numberUS09085576B2
Source datasetuspto-grants-2015_07
ORD IDord-c8f15a46f52d4dc494a0e6cdfd084270
Source noteuspto-grants-2015_07