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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629389Generated: October 30, 2026

Ethanol → [4-(1-methyl-1H-pyrazol-3-yl)phenyl]methanol

https://huagongshe.com/reaction/629389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantCesium carbonateHCID 10796—
Reactant4-(Hydroxymethyl)benzeneboronic acidHCID 2734706—
Reactant1-methyl-1H-pyrazol-3-yl trifluoromethanesulfonateHCID 117059543—
CatalystHCID 178418807HCID 178418807—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product[4-(1-methyl-1H-pyrazol-3-yl)phenyl]methanolHCID 2422946927.2%

Reaction Steps

A mixture of [4-(hydroxymethyl)phenyl]boronic acid (4.46 g), 1-methyl-1H-pyrazol-3-yl trifluoromethanesulfonate (4.50 g), cesium carbonate (19.1 g) and [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) dichloromethane adduct (0.80 g) in toluene (15.0 mL)-ethanol (1.00 mL)-water (1.00 mL) was subjected to microwave irradiation at 150° C. for 1 hr. The reaction mixture was diluted with ethyl acetate, and the insoluble substance was removed by filtration. The filtrate was washed successively with saturated aqueous sodium bicarbonate solution and saturated brine, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (1.00 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315458B2
Source datasetuspto-grants-2016_04
ORD IDord-19fc2cfce19b48379ea0303436522e96
Source noteuspto-grants-2016_04