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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505598Generated: November 4, 2026

4-Amino-5-iodo-2-(trifluoromethyl)benzonitrile → 4-Amino-5-cyano-2-trifluoromethyl-benzonitrile

https://huagongshe.com/reaction/505598

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-5-iodo-2-(trifluoromethyl)benzonitrileHCID 25067377—
ReactantHCID 178418546HCID 178418546—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product4-Amino-5-cyano-2-trifluoromethyl-benzonitrileHCID 16756857—

Reaction Steps

4-Amino-5-iodo-2-trifluoromethyl-benzonitrile (1.5 mmoL), CuCN (1.7 mmoL) in NMP (10 mL) was heated at 150° C. for 4 hrs. The reaction mixture was passed through a pad of Celite. The reaction mixture was then partitioned between ethyl acetate and water. The organic layer was washed with water, then brine, dried over anhydrous Na2SO4, filtered and concentrated to yield the title compound as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781473B2
Source datasetuspto-grants-2010_08
ORD IDord-2615f75ca54b424db1ba6911fc79518e
Source noteuspto-grants-2010_08