Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-(Trifluoromethoxy)phenylboronic acid | HCID 2734386 | — |
| Reactant | 3-(5-Bromo-2-thienyl)-2-propenoic acid | HCID 3565592 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 68537933 | HCID 68537933 | — |
Reaction Steps
0.72 g (3.1 mmol) of 3-(5-bromo-thiophen-2-yl)-acrylic acid and 178.3 mg (0.2 mmol) of tetrakis(triphenylphosphine)palladium were dissolved in 50 ml of degassed DME and stirred at room temperature for 10 min. 0.954 g (4.6 mmol) of 4-trifluoromethoxy-phenylboronic acid and 3 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. Solids were removed by filtration, and the filtrate was evaporated to dryness. The residue was dissolved in ethyl acetate and washed three times with a saturated sodium hydrogencarbonate solution and once with saturated sodium chloride solution. The organic phase was dried with sodium sulfate, filtered, and the solvent was removed under reduced pressure. Yield: 426 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08188291B2 |
|---|
| Source dataset | uspto-grants-2012_05 |
|---|
| ORD ID | ord-2a5e25be06434d86b691c5b8efcfee2d |
|---|
| Source note | uspto-grants-2012_05 |
|---|