Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Fluorophenylboronic acid | HCID 2734354 | — |
| Reactant | 3-(5-Bromo-2-thienyl)-2-propenoic acid | HCID 3565592 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 53412006 | HCID 53412006 | — |
Reaction Steps
9.38 g (40.2 mmol) of 3-(5-bromo-thiophen-2-yl)-acrylic acid and 6.97 g (6 mmol) of tetrakis(triphenylphosphine)palladium were dissolved in 50 ml of degassed DME and stirred at room temperature for 10 min. 8.44 g (60.4 mmol) of 2-fluoro -phenylboronic acid and 50 ml of a 2 M aqueous sodium carbonate solution were added together with an additional 5 ml of degassed DME. The reaction mixture was heated to 95° C. for 4 h and then stirred at room temperature for 16 h. The product precipitated partially from the reaction mixture and was collected by filtration. This solid was boiled for 1 h in ethyl acetate and filtered while hot. The solvent was removed under reduced pressure. The filtrate of the reaction mixture was evaporated to dryness. This residue was taken up in ethyl acetate/water and filtered. The organic phase was dried with sodium sulfate, filtered, and the solvent was evaporated. The combined product was purified by silica gel chromatography. Yield: 7.5 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188291B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-7a7c47cdc15942f9bec7721734b721c7 |
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| Source note | uspto-grants-2012_05 |
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