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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775270Generated: October 31, 2026

Dimethylformamide → 3-Amino-5-(trifluoromethyl)pyridine-2-carbonitrile

https://huagongshe.com/reaction/1775270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantEthyl AcetateHCID 8857—
Reactant2-Chloro-5-(trifluoromethyl)pyridin-3-amineHCID 12919757—
CatalystZinc cyanide (Zn(CN)2)HCID 11186—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
Product3-Amino-5-(trifluoromethyl)pyridine-2-carbonitrileHCID 13532251—

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 5.14 g of 3-amino-2-chloro-5-trifluoromethylpyridine, 3.92 g of zinc cyanide, 1.19 g of tris(dibenzylideneacetone)dipalladium(0), 1.45 g of 1,1′-bis(diphenylphosphino)ferrocene and 20 ml of DMF was stirred at 150° C. for 40 minutes. Ethyl acetate and water were added to the cooled reaction mixture, and the mixture was filtered. The aqueous layer of the filtrate was extracted with ethyl acetate, then combined with the organic layer of the filtrate and washed with water, and dried over anhydrous magnesium sulfate. The mixture was concentrated under reduced pressure, and then the resulting residue was applied to a silica gel column chromatography to obtain 2.23 g of 3-amino-2-cyano-5-trifluoromethylpyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260436B2
Source datasetuspto-grants-2016_02
ORD IDord-d4aa2b84fb7b4aea933d1f76df081531
Source noteuspto-grants-2016_02