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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1482865Generated: October 30, 2026

Water → 3-(Pyrimidin-2-ylmethoxy)-5-(4-(trifluoromethoxy)phenyl)benzo[d]isoxazole

https://huagongshe.com/reaction/1482865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Trifluoromethoxy)phenylboronic acidHCID 2734386—
Reactant5-Bromo-3-(pyrimidin-2-ylmethoxy)benzo[d]isoxazoleHCID 118161969—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product3-(Pyrimidin-2-ylmethoxy)-5-(4-(trifluoromethoxy)phenyl)benzo[d]isoxazoleHCID 11816188961.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

5-Bromo-3-(pyrimidin-2-ylmethoxy)benzo[d]isoxazole (120 mg, 0.39 mmol), 4-(trifluoromethoxy)phenylboronic acid (120 mg, 0.58 mmol), potassium carbonate (500 mg), and [1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II) (25 mg, 0.034 mmol) were combined in 6 mL DMF. 3 mL water was added and the mixture was stirred at 80° C. for two hours. The reaction mixture was diluted with 60 mL ethyl acetate, washed with water and brine and evaporated under vacuum. Flash chromatographic purification on 12 g silica gel with 0-60% ethyl acetate in hexane gave 3-(pyrimidin-2-ylmethoxy)-5-(4-(trifluoromethoxy)phenyl)benzo[d]isoxazole (94 mg, 0.24 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09416115B2
Source datasetuspto-grants-2016_08
ORD IDord-6dfb80fad55146fe8ab2a6bf9a0f441f
Source noteuspto-grants-2016_08