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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1160887Generated: November 3, 2026

Potassium Fluoride → HCID 67153562, compound

https://huagongshe.com/reaction/1160887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium FluorideHCID 522689—
Reactant4-tert-Butylphenylboronic acidHCID 2734320—
ReactantHCID 67153586HCID 67153586—
ReactantHCID 86615985HCID 86615985—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
SolventToluene waterHCID 22272177—
ProductHCID 67153562HCID 67153562—

Reaction Steps

To a solution of 3-{4-[1-(6-chloro-pyridin-3-yloxy)-4,4-dimethyl-pentyl]-benzoylamino}-propionic acid methyl ester (84 mg, 0.19 mmol) in toluene:water (1:1) (2 mL) is added palladium tetrakis triphenylphosphine (22.47 mg, 0.1 mol %), 4-tert-butylphenylboronic acid (58 mg, 0.39 mmol). The reaction is purged with nitrogen and heated to reflux and the potassium fluoride (23 mg, 0.39 mmol) is added. The reaction is monitored by HPLC, and upon completion, allowed to cool to room temperature. The reaction is diluted with ethyl acetate and then Celite is added, followed by water. This mixture is then filtered through a pad of Celite. The solution is separated in a seperatory funnel and the organic layer is washed with 0.1N sodium hydroxide, water, and brine. The organic layer is dried over anhydrous sodium sulfate and concentrated. The 5-(4-{1-[6-(4-tert-butyl-phenyl)-pyridin-3-yloxy]-4,4-dimethyl-pentyl}-phenyl)-5-oxo-pentanoic acid methyl ester (80 mg, 0.15 mmol) is purified by flash column chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07816557B2
Source datasetuspto-grants-2010_10
ORD IDord-2c9a97df693a4a42a800db5a4aa69751
Source noteuspto-grants-2010_10