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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862352Generated: October 30, 2026

Methyl Acrylate → HCID 44211033, compound

https://huagongshe.com/reaction/862352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl AcrylateHCID 7294—
Reactant1,3-Bis(diphenylphosphino)propaneHCID 81219—
ReactantHCID 21713099HCID 21713099—
Catalystpalladium(II) acetateHCID 167845—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
CatalystHCID 178418476HCID 178418476—
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) chloride (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 numberUS05716984
Source datasetuspto-grants-1998_02
ORD IDord-ea038faf92e8474db20a56d89cba1a9a
Source noteuspto-grants-1998_02