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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624392Generated: November 2, 2026

Phenylboronic Acid → HCID 66577647, compound

https://huagongshe.com/reaction/1624392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylboronic AcidHCID 66827—
ReactantTri-o-tolylphosphineHCID 80271—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 66577774HCID 66577774—
Catalystpalladium(II) acetateHCID 167845—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 66577647HCID 66577647—

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778983B2
Source datasetuspto-grants-2014_07
ORD IDord-ca501f04ea84433991473e61f1997b47
Source noteuspto-grants-2014_07