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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1533203Generated: November 3, 2026

2-Chloro-1-iodo-4-nitrobenzene → 2-Chloro-4-nitrobenzotrifluoride

https://huagongshe.com/reaction/1533203

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-1-iodo-4-nitrobenzeneHCID 96640—
ReactantPotassium FluorideHCID 522689—
Reactant(Trifluoromethyl)trimethylsilaneHCID 552549—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product2-Chloro-4-nitrobenzotrifluorideHCID 2778985—

Reaction Steps

A solution of 3-chloro-4-iodo-nitrobenzene (2.26 g), trimethyl(trifluoromethyl)silane (5.68 g), copper(I) iodide (2.28 g), and potassium fluoride (0.56 g) in N,N-dimethylformamide (8 mL) is heated in a sealed tube to 80° C. for 40 hours. The solution is then cooled, diluted with diethyl ether, filtered through diatomaceous earth, and the filtrate is washed successively with water, saturated aqueous sodium chloride, and then dried over anhydrous sodium sulfate. The solvent is removed under reduced pressure and the residue is chromatographed over silica gel (1% diethyl ether in hexanes followed by 10% ethyl acetate in hexanes is used as the eluant) to provided the desired product as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06207715B1
Source datasetuspto-grants-2001_03
ORD IDord-470754dfe0b040e1a8885aeb3ff3c7a6
Source noteuspto-grants-2001_03