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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388625Generated: October 30, 2026

Nitrogen → 1-(2,4-Dichlorobenzyl)-6-trifluoromethyl-1H-indazole-3-carboxylic Acid methyl ester

https://huagongshe.com/reaction/388625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
Reactant2,4-Dichlorobenzyl chlorideHCID 7212—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 6-(trifluoromethyl)-1H-indazole-3-carboxylateHCID 53408454—
CatalystTetrabutylammonium IodideHCID 67553—
SolventAcetonitrileHCID 6342—
Product1-(2,4-Dichlorobenzyl)-6-trifluoromethyl-1H-indazole-3-carboxylic Acid methyl esterHCID 11524204—

Reaction Steps

6-Trifluoromethyl-1H-indazole-3-carboxylic acid methyl ester (2.75 g, 0.0112 mol) was dissolved in acetonitrile (50 mL), and potassium carbonate (10 g, 0.07 mol), 2,4-dichlorobenzyl chloride (2.42 g, 0.01239 mol) and tetrabutylammonium iodide (catalytic) were added. The reaction mixture was heated to reflux and refluxed for 2 h under good stirring. The progress of the reaction was monitored by TLC. After completion of the reaction, potassium carbonate was filtered while hot and then washed with acetone. The combined solvents were distilled off under reduced pressure to afford the crude mixture of N1 and N2 benzylated products. The isomers were separated by column chromatography (silica gel, eluent started with hexane then changed to 8:2 hexane, ethyl acetate).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377958B2
Source datasetuspto-grants-2013_02
ORD IDord-7b72b867b9c04661a9bae994f8f73465
Source noteuspto-grants-2013_02