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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747708Generated: October 29, 2026

Sodium Iodide → 5-Iodo-2-(trifluoromethyl)benzonitrile

https://huagongshe.com/reaction/1747708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant5-Bromo-2-(trifluoromethyl)benzonitrileHCID 50998133—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
Product5-Iodo-2-(trifluoromethyl)benzonitrileHCID 66762150—

Reaction Steps

In a microwave vial 2.24 g 5-bromo-2-(trifluoromethyl)benzonitrile are dissolved in 10 ml 1,4-dioxane. 90 mg copper-(I)-iodide and 2.7 g sodium iodide are added and the mixture is purged for 5 minutes with argon. 142 μl trans-N,N′-dimet6hylcyclohexane-1,2-diamine and 1.9 ml hexamethyldisilazane are added and the mixture is heated for 6 hours to 110° C. The mixture is diluted in 100 ml 4 M hydrochloric acid and stirred for 10 minutes. This aqueous phase is three times extracted with dichloromethane. The combined organic phases are washed with brine and dried with magnesium sulphate. The solvents are evaporated in vacuo and the residue is chromatographed on silica gel (cyclohexane/ethylacetate 85:15).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150583B2
Source datasetuspto-grants-2015_10
ORD IDord-4daccad2bb814b3cb4a6ea459677ef07
Source noteuspto-grants-2015_10