HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624392Generated: November 2, 2026
Phenylboronic Acid → HCID 66577647, compound
https://huagongshe.com/reaction/1624392
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 66577774 | HCID 66577774 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 66577647 | HCID 66577647 | — |
Reaction Steps
1-{4′-[4-(4-Bromo-pyrazol-1-ylmethyl)-3-methyl-isoxazol-5-yl]-biphenyl-4-yl}-cyclopropanecarboxylic acid ethyl ester (0.062 g, 0.122 mmol), phenylboronic acid (0.018 g, 0.146 mmol), tri(o-tolyl)phosphine (0.004 g, 0.0122 mmol) and sodium bicarbonate (0.041 g, 0.488 mmol) were dissolved in DME (1.5 mL) and H2O (0.5 mL) and N2 (g) was bubbled through the mixture for 10 minutes. Palladium(II) acetate (1 mg, 0.002 mmol) was added and the reaction was heated to 90° C. for 1 hour. The reaction was cooled and purified via silica gel chromatography to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08778983B2 |
|---|
| Source dataset | uspto-grants-2014_07 |
|---|
| ORD ID | ord-ca501f04ea84433991473e61f1997b47 |
|---|
| Source note | uspto-grants-2014_07 |
|---|