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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1011570Generated: October 26, 2026

2'-Bromoacetophenone → 1-(2-Vinylphenyl)ethanone

https://huagongshe.com/reaction/1011570

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2'-BromoacetophenoneHCID 75060—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Ethenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 5233012—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product1-(2-Vinylphenyl)ethanoneHCID 22053669%

Reaction Conditions

Temperature95 °C

Reaction Steps

A solution of 2′-bromoacetophenone (1.6 mL, 12 mmol), sodium hydrogencarbonate (2.5 g, 30 mmol), vinylboronic acid pinacol ester (3.0 mL, 18 mmol) and tetrakis(triphenylphosphine)palladium(0) (0.69 g, 0.60 mmol) in a mixed solvent (50 mL), which consists of water and 1,4-dioxane (1:4), was stirred at 95° C. for 2.5 hours. Water (100 mL) was added to the reaction solution and extracted with ethyl acetate (100 mL). The organic layer was washed with brine (50 mL), dried over anhydrous magnesium sulfate. After the organic layer was filtered with celite and the solvent was removed under reduced pressure, the residue was purified by silica gel column chromatography to give the title reference compound (1.2 g) as an orange oil (Yield 69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977371B2
Source datasetuspto-grants-2011_07
ORD IDord-2c0d823e861149d7b49a2c42d8dc5305
Source noteuspto-grants-2011_07