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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767205Generated: October 26, 2026

Iodine → 1-(Benzyloxy)-2-iodo-4-(trifluoromethyl)benzene

https://huagongshe.com/reaction/1767205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSelectfluorHCID 2724933—
Reactant4-BenzyloxybenzotrifluorideHCID 2798168—
SolventAcetonitrileHCID 6342—
Product1-(Benzyloxy)-2-iodo-4-(trifluoromethyl)benzeneHCID 21112927158.2%

Reaction Steps

A solution of 4-(benzyloxy)benzotrifluoride (12.71 g, 50.4 mmol) in acetonitrile (300 ml) was stirred under nitrogen and 1-(chloromethyl)-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) (17.75 g, 50.4 mmol) and iodine (6.4 g, 25.2 mmol) added. The mixture was stirred at room temperature for 88 h. The solvent was evaporated and the residue partitioned between ethyl acetate (400 ml) and water (400 ml). The organic layer was washed with water, dried (MgSO4) and evaporated to an orange oil which was purified by flash chromatography (silica gel, 5% ethyl acetate: isohexane) to give the title compound as an orange oil (15.07 g, 79%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07232821B2
Source datasetuspto-grants-2007_06
ORD IDord-6149c89b2df84eb287255d0ce3ce4a24
Source noteuspto-grants-2007_06