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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2375753Generated: October 31, 2026

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

https://huagongshe.com/reaction/2375753

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 numberUS07465809B2
Source datasetuspto-grants-2008_12
ORD IDord-fb60a897a6e749d681644c3028839bab
Source noteuspto-grants-2008_12