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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166742Generated: November 2, 2026

Triethylamine → 2-[4-(2-Ethoxycarbonylvinyl)naphthyl]dioxolane

https://huagongshe.com/reaction/1166742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcrylateHCID 8821—
Reactant2-(4-Trifluoromethylsulfonyloxy naphthyl)dioxolaneHCID 54083125—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
Product2-[4-(2-Ethoxycarbonylvinyl)naphthyl]dioxolaneHCID 5368293353.7%

Reaction Conditions

Temperature90 °C

Reaction Steps

Nitrogen was passed through a solution of 2-(4-trifluoromethylsulfonyloxynaphthyl) dioxolane (2.46 g, 7.06 mmol), ethyl acrylate (2.3 mL, 2.1 g, 21.2 mmol), triethylamine (4.3 g, 42.3 mmol) in DMF (6 mL) for 15 min, and bis(triphenylphosphine)palladium dichloride was added. The well stirred solution was heated at 90° C. for 8 hr, and concentrated. The residue was dissolved in ethyl acetate (50 mL), washed with brine (2×50 mL), dried (Na2SO4), and concentrated. Purification by flash chromatography using hexane/ethyl acetate 9:1 as eluent provided a yellow solid (1.13 g, 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613942B1
Source datasetuspto-grants-2003_09
ORD IDord-ae5062cc5897487ab8c327f54d0e14e1
Source noteuspto-grants-2003_09