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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1861317Generated: November 2, 2026

Water → Methyl-2-fluoro-4-iodo-phenyl acetate

https://huagongshe.com/reaction/1861317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantEthyl AcetateHCID 8857—
Reactant2-(2-Fluoro-4-iodophenyl)acetonitrileHCID 22240532—
SolventBenzeneHCID 241—
SolventMethanolHCID 887—
SolventHexaneHCID 8058—
ProductMethyl-2-fluoro-4-iodo-phenyl acetateHCID 6954838380%

Reaction Steps

A solution of 2-fluoro-4-iodo-phenyl acetonitrile (Intermediate 2, 3 g, 11.45 mmol) in methanol (50 mL) and benzene (50 mL) was treated with p-toluene sulfonic acid (2.5 g, 13.15 mmol) and heated at reflux overnight using a Dean-Stark water trap. The volatiles were distilled off in vacuo and the residue was diluted with water and diethyl ether. The phases were separated and the organic phase was washed with saturated aqueous sodium bicarbonate (×1), water (×1) and brine (×1), dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo to afford an oil which was subjected to flash column chromatography over silica gel (230-400 mesh) using 6% ethyl acetate in hexane as the eluent to afford the title compound as a colorless oil (2.7 g, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06531599B2
Source datasetuspto-grants-2003_03
ORD IDord-5dc6e5497fc54b49ae9e36608700e129
Source noteuspto-grants-2003_03