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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521670Generated: October 30, 2026

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

https://huagongshe.com/reaction/521670

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 fixture, 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 numberUS09328121B1
Source datasetuspto-grants-2016_05
ORD IDord-5fb26c5e62e94e84b9e9dfd55fe3cf44
Source noteuspto-grants-2016_05