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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20330Generated: October 25, 2026

Vinyl Acetate → 1-Fluoro-2-(2-vinyloxyethyl)-benzene

https://huagongshe.com/reaction/20330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantVinyl AcetateHCID 7904—
ReactantSodium CarbonateHCID 10340—
Reactant2-(2-Fluorophenyl)ethan-1-olHCID 2733296—
CatalystChloro(1,5-cyclooctadiene)iridium(I) dimerHCID 6436381—
SolventTolueneHCID 1140—
Product1-Fluoro-2-(2-vinyloxyethyl)-benzeneHCID 6856353272.2%

Reaction Conditions

Temperature95 °C

Reaction Steps

Combine 2-(2-fluorophenyl)-ethanol (3.08 g, 22.0 mmol), vinyl acetate (4 mL, 43.3 mmol), anhydrous toluene (22 mL), chloro(1,5-cyclooctadiene)iridium(I) dimer (155 mg, 0.231 mmol), and anhydrous sodium carbonate (1.5 g, 14.2 mmol) in a dry round-bottom flask fitted with a reflux condensor under a nitrogen atmosphere. Heat the resulting mixture to 95° C. for 5 hours. Cool the reaction mixture to room temperature. Vacuum filter the resultant slurry to remove inorganic precipitates, washing the collected solid with hexanes. Concentrate and purify (silica gel chromatography, eluting with hexanes) to give the title compound as a yellow oil (2.64 g, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745438B2
Source datasetuspto-grants-2010_06
ORD IDord-7b1b0cb0cdd642c8a96a6098f2f2bb17
Source noteuspto-grants-2010_06