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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2185203Generated: October 30, 2026

Ethanol → Ethyl-2-fluoro-4-iodo-phenyl acetate

https://huagongshe.com/reaction/2185203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
ReactantSulfuric AcidHCID 1118—
Reactant2-(2-Fluoro-4-iodophenyl)acetic acidHCID 22240393—
Reactant2-Fluoro-iodo-phenyl acetic acidHCID 22568909—
SolventBenzeneHCID 241—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductEthyl-2-fluoro-4-iodo-phenyl acetateHCID 6954870173%

Reaction Steps

A solution of 2-fluoro-iodo-phenyl acetic acid (Intermediate 3, 1.75 g, 6.22 mmol) in ethanol (50 mL) and benzene (100 mL) was treated with concentrated sulfuric acid (1.4 mL) 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 5%-10% ethyl acetate in hexane as the eluent to afford the title compound as a pale yellow solid (1.4 g, 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06399774B1
Source datasetuspto-grants-2002_06
ORD IDord-fbc3dd3791664d51ab83e08d4425bd6d
Source noteuspto-grants-2002_06