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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256165Generated: October 25, 2026

Sodium Cyanide → 4-Cyano-3,5-dichloro-2,6-difluoropyridine

https://huagongshe.com/reaction/256165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
Reactant3,5-Dichloro-2,4,6-trifluoropyridineHCID 61273—
SolventDimethylformamideHCID 6228—
Product4-Cyano-3,5-dichloro-2,6-difluoropyridineHCID 1398516523.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 40.4 g (0.200 mole) of 3,5-dichloro-2,4,6-trifluoropyridine in 50 ml of dimethylformamide that had been cooled to 0° C. was added slowly 10 g (0.20 mole) of sodium cyanide. After addition was complete the reaction was stirred at 0° C. for two hours and at room temperature of two hours. The dimethylformamide was distilled from the reaction mixture under reduced pressure, and the black residue was mixed with 200 ml of water. This mixture was extracted with ethyl acetate. The extracts were combined, and the ethyl acetate was evaporated, leaving a black residue weighing approximately 15 g. This residue was distilled, yielding approximately 10 g of 4-cyano-3,5-dichloro-2,6-difluoropyridine as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04701464
Source datasetuspto-grants-1987_10
ORD IDord-add5cf799a0443cc96bae3a0187bdbc0
Source noteuspto-grants-1987_10