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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027171Generated: October 30, 2026

Salicylaldehyde oxime → (1-(4-bromo-3-methoxyphenyl)-1H-pyrazol-4-yl)methanol

https://huagongshe.com/reaction/1027171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalicylaldehyde oximeHCID 7200—
ReactantCesium carbonateHCID 10796—
Reactant4-HydroxymethylpyrazoleHCID 3015210—
Reactant2-Bromo-3-iodoanisoleHCID 23636210—
SolventDimethylformamideHCID 6228—
Product(1-(4-bromo-3-methoxyphenyl)-1H-pyrazol-4-yl)methanolHCID 8671056455.4%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 4-(hydroxymethyl)pyrazole (500 mg, 5.10 mmol), salicylaldoxime (140 mg, 1.019 mmol), cesium carbonate (4.98 g, 15.29 mmol), cuprous oxide (58.2 mg, 0.306 mmol), iodobromoanisole (1.59 g, 5.10 mmol) and N,N-dimethyl-formamide (10 mL) were combined in a microwave vial fitted with an N2 inlet and magnetic stir bar. The reaction mixture was stirred under a nitrogen atmosphere at 90° C. overnight. The reaction mixture was cooled to RT, then filtered through celite, and the filtrate was concentrated in vacuo. The crude material was purified by column chromotography (10% to 60% EtOAc in heptanes) to give (1-(4-bromo-3-methoxyphenyl)-1H-pyrazol-4-yl)methanol (800 mg, MS: 285.3 [M+H+].)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729263B2
Source datasetuspto-grants-2014_05
ORD IDord-2e83621e5fee4a4e85f60d0c7bd8d5e1
Source noteuspto-grants-2014_05