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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504469Generated: October 30, 2026

Potassium Carbonate → 3'-Chloro-3-fluoro-5-methoxy-1,1'-biphenyl

https://huagongshe.com/reaction/1504469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(3-Chlorophenyl)boronic acidHCID 2734323—
Reactant3-Bromo-5-fluoroanisoleHCID 10822094—
CatalystHCID 178418397HCID 178418397—
Product3'-Chloro-3-fluoro-5-methoxy-1,1'-biphenylHCID 117737212102%

Reaction Steps

A RBF was charged with 1-bromo-3-fluoro-5-methoxybenzene (2.104 g, 10.26 mmol), (3-chlorophenyl)boronic acid (1.765 g, 11.29 mmol), potassium carbonate (4.25 g, 30.8 mmol), and Pd(Ph3P)4 (0.593 g, 0.513 mmol). The flask was flushed with Ar (g), then 1,4-dioxane (25.7 ml) and water (8.55 ml) were added. A reflux condenser was attached, and the flask was lowered into a 90° C. heating bath for 45 min. The mixture was cooled to room temperature, diluted with water, and extracted with EtOAc (2×). The combined organic extracts were dried over sodium sulfate, filtered, and concentrated. The residue was purified by chromatography on silica gel (50-g SNAP Ultra column, 25-g silica gel column, 0-5% EtOAc/Heptane) to give 3′-chloro-3-fluoro-5-methoxy-1,1′-biphenyl (2.47 g, 10.44 mmol, 102% yield) as a clear oil containing about 10 wt % impurities.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212182B2
Source datasetuspto-grants-2015_12
ORD IDord-374895cbf32747ee9287aecee0f669da
Source noteuspto-grants-2015_12