Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166072Generated: October 29, 2026

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

https://huagongshe.com/reaction/1166072

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 hexane/ethyl 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) δ 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 numberUS06613765B1
Source datasetuspto-grants-2003_09
ORD IDord-a0c13e8ec4394029be7a63e6858c7187
Source noteuspto-grants-2003_09