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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485511Generated: November 1, 2026

2,6-Dichloro-3-nitropyridine → 6-Chloro-3-nitropyridine-2-carbonitrile

https://huagongshe.com/reaction/1485511

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Dichloro-3-nitropyridineHCID 85239—
ReactantHCID 178418546HCID 178418546—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product6-Chloro-3-nitropyridine-2-carbonitrileHCID 1338170544.5%

Reaction Conditions

Temperature180 °C

Reaction Steps

To a solution of 2,6-dichloro-3-nitropyridine (6.00 g, 31.1 mmol) in NMP (23.0 mL) was added copper(I) cyanide (3.06 g, 34.2 mmol) at room temperature. After stirred for 40 min at 180° C., the reaction mixture was cooled to room temperature, and then poured into ice water. After stirring for 10 min, the mixture was extracted with EtOAc, washed with brine, dried over anhydrous Na2SO4, filtered and concentrated in vacuo. The residue was purified by column chromatography on SiO2 (Hex:EtOAc=10:1) to give 6-chloro-3-nitropicolinonitrile (2.54 g, 44%) as a yellow solid. 1H-NMR (CDCl3, Varian 400 MHz) δ 7.79 (1H, d, J=8.4 Hz), 8.58 (1H, d, J=8.4 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422298B2
Source datasetuspto-grants-2016_08
ORD IDord-4de656b40a284869bf188497b4d790c8
Source noteuspto-grants-2016_08