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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902203Generated: October 30, 2026

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

https://huagongshe.com/reaction/902203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhenyl dihydrogen orthoborateHCID 78412—
ReactantHCID 178524955HCID 178524955—
CatalystCupric acetateHCID 8895—
SolventChlorideHCID 312—
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) inmethylene 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 numberUS07365079B2
Source datasetuspto-grants-2008_04
ORD IDord-d2db3cb206df4545b8f69fad5ff6b560
Source noteuspto-grants-2008_04