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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403762Generated: November 1, 2026

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

https://huagongshe.com/reaction/2403762

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 numberUS08802637B2
Source datasetuspto-grants-2014_08
ORD IDord-96a771943bc54af388e67c7aa7705a94
Source noteuspto-grants-2014_08