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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198761Generated: October 31, 2026

Methane → 2-(1H-pyrazol-1-yl)aniline

https://huagongshe.com/reaction/2198761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
Reactant1-(2-Nitrophenyl)-1H-pyrazoleHCID 605016—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product2-(1H-pyrazol-1-yl)anilineHCID 277971090%

Reaction Steps

Into a Parr hydrogenation apparatus is successively added 20 g. (0.106 M.) of 1-(o-nitrophenyl)-pyrazole and 150 ml. of methanol and the resultant solution is hydrogenated in the presence of 1.0 g. of hydrogenation catalyst (10% Pd on active charcoal) at between 40 and 50 p.s.i. of hydrogen pressure at room temperature. After the theoretical uptake of hydrogen is achieved, the reaction mixture is filtered to remove the palladium and the solvent is removed on a rotary evaporator. Ether is then added to the resultant mixture and after removing the precipitated solids by filtration, the solvent is evaporated to yield a light amber colored oil (Yield: 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04359474
Source datasetuspto-grants-1982_11
ORD IDord-4b1bac9c52464d0389322ae5252885cb
Source noteuspto-grants-1982_11