HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984352Generated: October 29, 2026
Sodium Carbonate → (E)-ethyl 3-(4-furan-2-yl-phenyl)-but-2-enoate
https://huagongshe.com/reaction/984352
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Furan-2-boronic acid | HCID 2734357 | — |
| Reactant | (E)-ethyl 3-(4-iodophenyl)-but-2-enoate | HCID 11438459 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | (E)-ethyl 3-(4-furan-2-yl-phenyl)-but-2-enoate | HCID 22557549 | — |
Reaction Steps
Tetrakis(triphenylphoshine)palladium(0) (0.69 g, 0.60 mmol, 6 mol %) was added, under nitrogen, to a stirred solution of (E)-ethyl 3-(4-iodophenyl)-but-2-enoate (3.16 g, 10.0 mmol) in DME (100 ml), and the resulting orange coloured solution stirred at room temperature for 10 min. Aqueous 2M sodium carbonate (30.0 ml, 60.0 mmol) was then added, the mixture stirred for 10 min, then furan-2-boronic acid (2.25 g, 20.11 mmol) was added, and the reaction mixture heated to 80° C. for 20 h, under reflux. The reaction mixture was cooled, diluted with water (100 ml) and the products extracted into ethyl acetate (3×100 ml). The combined organic extracts were washed with brine, dried (MgSO4), and evaporated to give the crude product, which was purified by column chromatography on silica gel (3% diethyl ether in n-heptane eluent) to give the product, (E)-ethyl 3-(4-furan-2-yl-phenyl)-but-2-enoate as an off-white solid; 2.46 g (96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06867218B2 |
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| Source dataset | uspto-grants-2005_03 |
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| ORD ID | ord-5a9380a62c5e4891b429ae0f74105b64 |
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| Source note | uspto-grants-2005_03 |
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