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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650773Generated: October 29, 2026

Methyl Acrylate → HCID 44211033, compound

https://huagongshe.com/reaction/650773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl AcrylateHCID 7294—
Reactant1,3-Bis(diphenylphosphino)propaneHCID 81219—
ReactantHCID 21713099HCID 21713099—
Catalystpalladium(II) acetateHCID 167845—
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(II) 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 numberUS06274737B1
Source datasetuspto-grants-2001_08
ORD IDord-e87becb563eb4dd6b4e3042db79593c4
Source noteuspto-grants-2001_08