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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898490Generated: October 30, 2026

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

https://huagongshe.com/reaction/898490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropenyl acetateHCID 7916—
ReactantTri-o-tolylphosphineHCID 80271—
ReactantMethyl 2-(3-bromophenyl)acetateHCID 11746402—
ReactantMethoxytri-n-butylstannaneHCID 11964040—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
SolventPotassium FluorideHCID 522689—
ProductMethyl [3-(2-oxopropyl)phenyl]acetateHCID 21035403—

Reaction Steps

Tributyltin methoxide (28.3 ml, 98 mmol), methyl (3-bromophenyl)acetate (WO 95/27692, pg. 16, e.g. 5a) (15.0 g, 65.0 mmol), isopropenyl acetate (10.8 ml, 98.0 mmol), palladium(II)acetate (750 mg, 3.30 mmol) and tri-ortho-tolylphosphine (2.0 g, 6.5 mmol) were stirred together in toluene (75 ml) at 100° C. under nitrogen for 5 hours. After cooling the reaction was diluted with ethyl acetate (150 ml) and 4M aqueous potassium fluoride solution (90 ml) and stirred for 15 minutes. The mixture was filtered through Arbocel® and the organic phase separated and concentrated in vacuo. The residue was purified column chromatography on silica gel eluting with diethyl ether:pentane (0:100 to 25:75 and then changing to dichloromethane), to yield the title compound as a pale yellow oil, 12.6 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07351742B2
Source datasetuspto-grants-2008_04
ORD IDord-10a691ca20304f518b71afe79a1cc4ee
Source noteuspto-grants-2008_04