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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027180Generated: October 30, 2026

Salicylaldehyde oxime → HCID 86710575, compound

https://huagongshe.com/reaction/1027180

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalicylaldehyde oximeHCID 7200—
ReactantCesium carbonateHCID 10796—
Reactant1-Bromo-4-iodo-2-methoxybenzeneHCID 12187202—
ReactantHCID 178526745HCID 178526745—
SolventDimethylformamideHCID 6228—
ProductHCID 86710575HCID 8671057560.5%

Reaction Conditions

Temperature95 °C

Reaction Steps

A mixture of 1-bromo-4-iodo-2-methoxybenzene (3.99 g, 12.75 mmol), 3-nitro-1H-pyrazole (1.730 g, 15.30 mmol), Salicylaldoxime (0.350 g, 2.55 mmol), Cu2O (0.146 g, 1.020 mmol) and Cs2CO3 (6.23 g, 19.13 mmol) in DMF (13 mL) was degassed with N2 and heated at 95° C. overnight. After cooling to RT, the mixture was filtered through celite and rinsed with EtOAc. The filtrate was washed with water and brine. The organic solution was dried over Na2SO4, filtered and concentrated in vacuo. The residue was suspended in 5% MeOH/DCM, and the precipitate filtered, rinsed with 5% MeOH/DCM, and dried to give 2.3 g of 1-(4-bromo-3-methoxyphenyl)-3-nitro-1H-pyrazole as a white solid. The filtrate from the above work up was purified by silica gel chromatography (EtOAc/Heptane=10:90 to 50:50) to give an additional 760 mg of 1-(4-bromo-3-methoxyphenyl)-3-nitro-1H-pyrazole as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729263B2
Source datasetuspto-grants-2014_05
ORD IDord-4806e4de634243e1bc28cb14f19ae4d2
Source noteuspto-grants-2014_05