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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097028Generated: November 1, 2026

Isopropenyl acetate → Methyl [3-(2-oxopropyl)phenyl]acetate

https://huagongshe.com/reaction/1097028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropenyl acetateHCID 7916—
ReactantTri-o-tolylphosphineHCID 80271—
ReactantPotassium FluorideHCID 522689—
ReactantMethyl 2-(3-bromophenyl)acetateHCID 11746402—
ReactantMethoxytri-n-butylstannaneHCID 11964040—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductMethyl [3-(2-oxopropyl)phenyl]acetateHCID 2103540366.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

A stirred mixture of methyl (3-bromophenyl)acetate (19.7 g, 86.0 mmol), tributyltin methoxide (37.1 mL, 129 mmol), isopropenyl acetate (14.2 mL, 129 mmol), palladium acetate (961 mg, 4.28 mmol), and tri-o-tolylphosphine (2.63 g, 8.64 mmol) in toluene (70 mL) was heated at 100° C. for 6 h. Aqueous potassium fluoride solution (4 M, 120 mL) and EtOAc (200 mL) were added and the resulting mixture was stirred overnight. The mixture was then filtered through Celite and the layers were separated. The organic layer was washed with water and then concentrated under reduced pressure. The residue was purified by silica gel flash chromatography (0-8% MeOH in DCM) to give the title compound (11.8 g, 66% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138345B2
Source datasetuspto-grants-2012_03
ORD IDord-88ba81ec8a24445f8c6f2b624330d1c9
Source noteuspto-grants-2012_03