Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119442Generated: November 3, 2026

Pyridine → HCID 22728884, compound

https://huagongshe.com/reaction/2119442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant1,1'-Biphenyl-4-yl-boronic acidHCID 151253—
ReactantHCID 178469061HCID 178469061—
CatalystCupric acetateHCID 8895—
SolventDichloromethaneHCID 6344—
ProductHCID 22728884HCID 2272888426%

Reaction Steps

To a solution of 4-biphenylboronic acid (1.0 g, 5.1 mmol) and ethyl 3-methylpyrazole-5-carboxylate (0.78 g, 5.1 mmol) in 25 mL dry DCM were added pyridine (1.2 mL, 15 mmol) and anhydrous powder of copper(II) acetate (1.84 g, 10 mmol). Some activated molecular sieve powder was added afterwards. The resulting slurry was refluxed for 2 days under argon. The mixture was diluted with DCM, filtered through celite. The blue filtrate was washed with water (×2), dried, concentrated, purified with flush column to yield ethyl 3-methyl-1-(4-phenylphenyl)-1H-pyrazole-5-carboxylate (26%), Rf 0.67 (1:2 EtOAc:hexane), ES-MS: (M+H)+ 307; and its regioisomer, ethyl 5-methyl-1-(4-phenylphenyl)-1H-pyrazole-3-carboxylate (31%), Rf 0.50 (1:2 EtOAc:hexane), ES-MS: (M+H)+ 307.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06686368B1
Source datasetuspto-grants-2004_02
ORD IDord-a1816d33f1074bda82f55ea71eaceb47
Source noteuspto-grants-2004_02