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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1600666Generated: November 1, 2026

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

https://huagongshe.com/reaction/1600666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant2-Benzyloxy-5-(trifluoromethoxy)benzeneHCID 21584094—
CatalystSilver trifluoroacetateHCID 76299—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
Product1-(Benzyloxy)-2-iodo-4-(trifluoromethoxy)benzeneHCID 11395278101.5%

Reaction Steps

Iodine (71.96 g, 0.28 mol) in chloroform was added dropwise to a mixture of 2-benzyloxy-5-(trifluoromethoxy)benzene (Preparation 12, 73.06 g, 0.27 mol) and silver trifluoroacetate (71.57 g, 0.32 mol) in dichloromethane and the mixture was stirred at room temperature for 18 hours. The mixture was filtered through celite, washed with aqueous sodium thiosulfate (5%, 2×2 l), dried (MgSO4) and the solvent was evaporated under reduced pressure. The residue was purified by flash column chromatography on silica gel, eluting with hexanelethyl acetate, to give the title compound as a colorless oil (108.03 g), containing 11% unreacted 2-benzyloxy-5-(trifluoromethoxy)iodobenzene. 1H NMR (360 MHz, CDCl3) 8 7.67 (1H, d, J=2.8 Hz), 7.40 (5H, m), 7.16 (1H, dd, J=8.9, 2.8 Hz), 6.82 (1H, d, J=8.9 Hz), and 5.14 (2H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977104
Source datasetuspto-grants-1999_11
ORD IDord-0716cc425b8243ebbb5eca022d325ba7
Source noteuspto-grants-1999_11