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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | 2-(4-Trifluoromethylsulfonyloxy naphthyl)dioxolane | HCID 54083125 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-[4-(2-Ethoxycarbonylvinyl)naphthyl]dioxolane | HCID 53682933 | 53.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06613942B1 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-ae5062cc5897487ab8c327f54d0e14e1 |
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| Source note | uspto-grants-2003_09 |
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