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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912831Generated: November 1, 2026

Iodine → 4-Iodo-6-(trifluoromethyl)-1,3-dihydro-2H-benzimidazol-2-one

https://huagongshe.com/reaction/912831

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantIsoamyl NitriteHCID 8053—
ReactantCesium iodideHCID 24601—
Reactant4-Amino-6-trifluoromethyl-1,3-dihydro-benzoimidazol-2-oneHCID 67401137—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDichloromethaneHCID 6344—
Product4-Iodo-6-(trifluoromethyl)-1,3-dihydro-2H-benzimidazol-2-oneHCID 67401177—

Reaction Conditions

Temperature60 °C

Reaction Steps

(Analogous to the procedure described in Heterocycles, 2001, 55, 461-464). To a solution of 4-amino-6-(trifluoromethyl)-1,3-dihydro-2H-benzimidazol-2-one from step (a) above (0.76 g, 3.5 mmol) in 20 mL of DCM was added CsI (0.91 g, 3.5 mmol), I2 (0.44 g, 1.75 mmol), and CuI (0.2 g, 1.06 mmol). To the mixture was added isoamyl nitrite (2.8 mL, Aldrich) and the reaction mixture was heated at 60° C. with stirring for 3 h. The reaction mixture was cooled to room temperature, filtered, and the filtrate was diluted with EcOAc (60 mL). The solution was washed with 25% NH4OH (2×30 mL), 5% Na2S2O3 (20 mL) and brine, dried over MgSO4 and filtered. The filtrate was evaporated and the residue was purified by silica gel column chromatography, eluting with 30% EtOAc/hexane to give the title compound as a brown solid. MS (ESI, pos. ion) m/z: 329 (M+1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026241B2
Source datasetuspto-grants-2011_09
ORD IDord-1e3e3d10465049e39e8b9f7fde21cc91
Source noteuspto-grants-2011_09