Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | HCID 66616129 | HCID 66616129 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 11501024 | HCID 11501024 | 79.2% |
Reaction Steps
A 10 mL glass tube with a stirbar is charged with methyl 3-[1-(4-bromo-phenyl)-1H-[1,2,4]triazol-3-yl]-benzoate (265 mg, 0.74 mmol), benzeneboronic acid (90.2 mg, 0.74 mmol), sodium carbonate (235 mg), tetrabutylammonium iodide (273 mg), palladium acetate (0.8 mg) and 6 mL water. The vessel is sealed and placed into the reaction cavity of a microwave reactor. The reaction is performed with 60 W power at 150° C., with monitoring by LC/MS. After the reaction is determined to be complete, the mixture is filtered through celite and acidified using 1N HCl until the pH of the medium is less than 7. The resulting solid is collected by filtration and recrystallized to purity from THF-hexane to afford the title product (200 mg, 79%) as a white powder, m.p. 263-265° C. 1H NMR (300 MHz, DMSO-d6): δ 9.47 (1H, s), 8.69 (1H, s), 8.34 (1H, d, J=7.5 Hz), 8.05-7.39 (1H, m). MS (ES+): m/e 343 (30), 342 (100).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051342B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-9bdc7f8977984fa599c889dc32706080 |
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| Source note | uspto-grants-2015_06 |
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