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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183932Generated: November 1, 2026

Potassium Acetate → 2,4-Difluoro-3-(pyridin-3-yl)benzeneboronic acid

https://huagongshe.com/reaction/2183932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium AcetateHCID 517044—
ReactantBis(neopentyl glycolato)diboronHCID 2734316—
Reactant3-(3-Bromo-2,6-difluorophenyl)pyridineHCID 22240086—
Solvent1,4-DioxaneHCID 31275—
Product2,4-Difluoro-3-(pyridin-3-yl)benzeneboronic acidHCID 2224009685.1%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 3-(3-bromo-2,6-difluorophenyl)pyridine (2.97 g, 11 mmol), potassium acetate (2.16 g, 22 mmol) and bis(neopentyl glycolato)diboron (2.86 g, 12.7 mmol) in 1,4-dioxane (30 ml) was heated at 90° C. for 16 h. The reaction was cooled, filtered (washing the filter cake with a small quantity of diethyl ether) and the filtrate concentrated in vacuo. The residue was partitioned between diethyl ether (100 ml) and 1M sodium hydroxide (100 ml) and the organics discarded. The aqueous was washed with more diethyl ether and then cooled in an ice-water bath. The pH was adjusted to approximately 6 with 36% hydrochloric acid, and allowed to stand for 1 h. The resulting solid was collected by filtration and dried under vacuum to afford 2,4-difluoro-3-(pyridin-3-yl)benzeneboronic acid (2.2 g, 85%) as a grey solid: m/z (ES+) 236 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900215B2
Source datasetuspto-grants-2005_05
ORD IDord-55487be94dd14405850fedc9b86e69d3
Source noteuspto-grants-2005_05