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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228522Generated: October 29, 2026

Trifluoroacetic anhydride → 2-Cyano-4,5-dimethoxy-3-(2,2,2-trifluoroethoxy)nitrobenzene

https://huagongshe.com/reaction/2228522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantAmmonium nitrateHCID 22985—
Reactant3,4-Dimethoxy-2-(2,2,2,-trifluoroethoxy)benzonitrileHCID 18470636—
SolventDichloromethaneHCID 6344—
Product2-Cyano-4,5-dimethoxy-3-(2,2,2-trifluoroethoxy)nitrobenzeneHCID 1847061973%

Reaction Steps

Ammonium nitrate (2.82 g, 0.035 mol) and trifluoroacetic anhydride (12.4 ml, 0.088 mol) were added to a solution of 3,4-dimethoxy-2-(2,2,2,-trifluorethoxy)benzonitrile in dichloromethane. The temperature was maintained between 20° C. and 30° C. for 2 hours, after which time the reaction mixture was washed with saturated aqueous sodium bicarbonate solution. The organic layer was separated, dried (MgSO4) and evaporated under reduced pressure. Trituration with diethyl ether followed by filtration afforded a first crop of product. The filtrate was purified on silica gel, eluting with dichloromethane to afford the subtitle compound as a colourless solid (combined yield 6.56 g, 73%). Rf 0.31 (ethyl acetate:hexane 20:80, v/v). MS m/z 324 (MNH4)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06417194B1
Source datasetuspto-grants-2002_07
ORD IDord-16df20eee4f5477c9df9eb6656422042
Source noteuspto-grants-2002_07