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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957271Generated: October 27, 2026

Water → 3-Chloro-2-(4-cyano-3-nitrophenyl)-5-trifluoromethylpyridine

https://huagongshe.com/reaction/1957271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CyanideHCID 9032—
Reactant3-Chloro-2-(4-fluoro-3-nitrophenyl)-5-(trifluoromethyl)pyridineHCID 22114842—
SolventDimethylformamideHCID 6228—
Product3-Chloro-2-(4-cyano-3-nitrophenyl)-5-trifluoromethylpyridineHCID 19068752—

Reaction Conditions

Temperature23 °C

Reaction Steps

5.0 g of 3-chloro-2-(4-fluoro-3-nitrophenyl)-5-trifluoromethylpyridine and 1.5 g of potassium cyanide in 50 ml of dimethylformamide were heated at 50° C. for 4 hours and then stirred at 23° C. for 20 hours. The mixture was then poured into 200 ml of water. The aqueous phase was extracted three times with 100 ml of tertbutyl methyl ether each time. The combined organic phases were washed twice with 50 ml of water each time, dried over sodium sulfate and concentrated. The residue was purified by chromatography on silica gel (mobile phase: cyclohexane/ethyl acetate=9:1). Yield: 2.7 g (53%) of a yellow oil which slowly crystallized.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05783522
Source datasetuspto-grants-1998_07
ORD IDord-6ede41fbbc33493494ca78ea9791b82c
Source noteuspto-grants-1998_07