HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444205Generated: October 31, 2026
Potassium Carbonate → HCID 68497799, compound
https://huagongshe.com/reaction/1444205
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (4-Methoxyphenyl)boronic acid | HCID 201262 | — |
| Reactant | HCID 59654709 | HCID 59654709 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Catalyst | Palladium (II) acetate | HCID 4144353 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 68497799 | HCID 68497799 | 92.8% |
Reaction Steps
To a previously degassed mixture of (3-[(5-bromo-furan-2-carbonyl)-amino]-phenyl)-acetic acid ethyl ester (11) (0.4 g), 4-methoxyphenylboronic acid (0.19 g), potassium carbonate (0.39 g) and tetra-n-butylammonium bromide (0.37 g) in water (2 ml) was added palladium II acetate (circa 10 mg). The mixture was heated to 70° C. for an hour, cooled and partitioned between ethyl acetate and water. The organic layer was separated, washed with brine, dried over sodium sulphate and evaporated in vacuo. (3-[(5-(4-Methoxy-phenyl)-furan-2-carbonyl)-amino]-phenyl)-acetic acid ethyl ester (0.4 g) was obtained following silica gel column chromatography of the residue in 2:1 ethyl acetate:petroleum ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07662839B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-7b9551fda5be45a7b6f6f6b96fd585f6 |
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| Source note | uspto-grants-2010_02 |
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