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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733117Generated: October 31, 2026

Pyridine → methyl 4-nitro-1-phenyl-1H-pyrazole-3-carboxylate

https://huagongshe.com/reaction/733117

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhenyl dihydrogen orthoborateHCID 78412—
ReactantHCID 178524955HCID 178524955—
CatalystCupric acetateHCID 8895—
SolventDichloromethaneHCID 6344—
Productmethyl 4-nitro-1-phenyl-1H-pyrazole-3-carboxylateHCID 2308489783.8%

Reaction Steps

To a solution of 4-nitro-1H-pyrazole-3-carboxylate (1.0 g, 5.84 mmol) in methylene chloride (20 mL) were added phenylboric acid (1.43 g, 11.7 mmol), copper(II) acetate (1.60 g, 8.76 mmol) and pyridine (2 mL, 23.4 mmol), and the mixture was stirred overnight at room temperature under an air atmosphere. After removal of the insolubles by filtration, the filtrate was washed with water (twice) and saturated brine, dried over anhydrous magnesium sulfate and concentrated in vacuo to obtain the title compound (1.21 g, 83.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07589096B2
Source datasetuspto-grants-2009_09
ORD IDord-86bc90e3542c49b6800c68c6eec4cc6f
Source noteuspto-grants-2009_09