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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660978Generated: October 31, 2026

Water → 6-(4-tert-Butylphenyl)pyridin-3-ol

https://huagongshe.com/reaction/660978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium FluorideHCID 522689—
Reactant2-Chloro-5-hydroxypyridineHCID 819821—
Reactant4-tert-Butylphenylboronic acidHCID 2734320—
SolventTolueneHCID 1140—
Product6-(4-tert-Butylphenyl)pyridin-3-olHCID 5322943337.9%

Reaction Steps

To a solution of 6-Chloro-pyridin-3-ol (3.10 g, 23.9 mmol) in toluene (30 ml) is added 4-tert-butyl-phenylboronic acid (5.46 g, 30.6 mmol), potassium fluoride (2.82 g, 47.9 mmol), and palladium tetrakis triphenylphosphine (1.20 g, 1.20 mmol). Water (15 mL) is added and the reaction mixture is heated to reflux overnight. After cooling to rt, the reaction mixture is partitioned between ethyl acetate and water. The aqueous layer is back-extracted with ethyl acetate, the combined organic layers are dried and concentrated. The resulting residue is applied to silica gel and eluted using hexanes with an ethyl acetate gradient to give the title compound (2.06 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084489B2
Source datasetuspto-grants-2011_12
ORD IDord-e97e9f3583d249c9b13a20442345978f
Source noteuspto-grants-2011_12