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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650416Generated: October 30, 2026

Acetate → HCID 44211033, compound

https://huagongshe.com/reaction/650416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetateHCID 175—
ReactantMethyl AcrylateHCID 7294—
Reactant1,3-Bis(diphenylphosphino)propaneHCID 81219—
ReactantHCID 21713099HCID 21713099—
CatalystPalladiumHCID 23938—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventDimethylformamideHCID 6228—
SolventAcetonitrile triethylamineHCID 21895542—
ProductHCID 44211033HCID 44211033—

Reaction Steps

1,3-bis(diphenylphosphino)propane (0.066 mmol), tris(dibenzylideneacetone)-dipalladium(0) (24 mg, 0.026) and bis(triphenylphosphine)palladium(II) choride (18 mg, 0.026 mmol), were dissolved in a 4:1 mixture of triethylamine/acetonitrile (5 mL) under argon. After 10 min at room temperature, a solution of methyl (1RS, 2SR, 3RS)-3-(4-methoxy-2-trifluoromethanesulfonyloxyphenyl)-1-(3,4-methylenedioxyphenyl)-5-(prop-1-yloxy)indane-2-carboxylate (160 mg, 0.26 mmol) and methyl acrylate (679 mg, 7.89 mmol) was added in the above solvent mixture (3 mL). The reaction mixture was heated to reflux under argon for 20 h, cooled to room temperature and a small aliquot analyzed by 1H NMR, which showed no reaction had taken place. Palladium(l) acetate (6 mg, 0.025 mmol) and methyl acrylate (679 mg, 7.89 mmol) in dry DMF (5 mL) were then added. The reaction mixture was heated to reflux overnight. On cooling the solution was filtered through a short column of silica gel and concentrated to yield an oil. The crude product was purified by flash column chromatography ( silica gel, gradient elution: 10% to 20% ethyl acetate/hexanes) to afford the title compound as a tan solid. (87 mg, 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06271399B1
Source datasetuspto-grants-2001_08
ORD IDord-007f3a477145488095844fdccdf1e1f0
Source noteuspto-grants-2001_08