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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425085Generated: October 30, 2026

Vinyl Acetate → 4-Bromo-1-chloro-2-(4-(2-(vinyloxy)ethyl)benzyl)benzene

https://huagongshe.com/reaction/425085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantVinyl AcetateHCID 7904—
ReactantSodium CarbonateHCID 10340—
Reactant2-(4-(5-Bromo-2-chlorobenzyl)phenyl)ethanolHCID 59557766—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product4-Bromo-1-chloro-2-(4-(2-(vinyloxy)ethyl)benzyl)benzeneHCID 5955777286.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 2-(4-(5-bromo-2-chlorobenzyl)phenyl)ethanol (intermediate BH) (500 mg, 1.46 mmol), [IrCl(cod)]2 (9.8 mg, 0.015 mmol) and sodium carbonate (93 mg, 0.87 mmol) in toluene (2 mL) was added vinyl acetate (0.27 mL, 2.91 mmol) under argon. The reaction mixture was heated to 100° C. and stirred for 2 h. The solution was allowed to cool to room temperature, and then diluted with 50 mL of ethyl acetate. The mixture was washed with water (20 mL) and then with brine (20 mL), and dried over sodium sulfate. The residue was concentrated and purified by column chromatography (eluent EA:PE:Et3N=1:20:0.01) to provide 445 mg of yellow solid. 1H-NMR (CDCl3, 400 MHz): δ 7.22˜7.14 (m, 3H), 7.10 (d, 2H), 7.04 (d, 2H), 6.40 (dd, J=14.4 and 6.8 Hz, 1H), 4.11 (dd, J=14.4 and 2.0 Hz, 1H), 3.96 (s, 2H), 3.93 (dd, J=6.8 and 2.0 Hz, 1H), 3.82 (t, J=7.2 Hz, 2H), 2.88 (t, J=7.2 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106021B2
Source datasetuspto-grants-2012_01
ORD IDord-d5e12efae06c44f7bf8d5dfe1267e602
Source noteuspto-grants-2012_01