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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038118Generated: November 4, 2026

Ethanol → 2-(4-Bromo-2,3-difluoro-phenyl)-pyrimidine

https://huagongshe.com/reaction/1038118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium CarbonateHCID 11430—
Reactant2-BromopyrimidineHCID 78345—
Reactant4-Bromo-2,3-difluorobenzeneboronic acidHCID 2773292—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product2-(4-Bromo-2,3-difluoro-phenyl)-pyrimidineHCID 57685931—

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 2-bromopyrimidine (2.0 g, 12.7 mmol), 4-bromo-2,3-difluorobenzeneboronic acid (1.0 g, 4.22 mmol), potassium carbonate (2.93 g, 21.1 mmol) in a mixture of toluene (30 ml)/ethanol (30 ml)/water (15 ml) were purged with nitrogen for 15 min. Tetrakis(triphenylphosphine)palladium(0) (488 mg, 0.42 mmol) was added and the mixture was stirred at 90° C. in a sealed-tube for overnight. The mixture was cooled to r.t. and was diluted with water and ethyl acetate. Layers were separated. The separated organic layer was dried (MgSO4), filtered and solvents were removed in vacuum. Column purification [Hexanes-Ethyl acetate, 2:1 (v/v)] gave bromide 3AC (0.97 g, 85%) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546404B2
Source datasetuspto-grants-2013_10
ORD IDord-5414e2b09a2c40629eb0f0a956f0615b
Source noteuspto-grants-2013_10