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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2384007Generated: October 31, 2026

Water → HCID 59192524, compound

https://huagongshe.com/reaction/2384007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromo-2-chloropyridineHCID 2734414—
Reactant3-Isopropylbenzeneboronic acidHCID 2773478—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
ProductHCID 59192524HCID 5919252459%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution of 5-bromo-2-chloropyridine (1.27 g, 6.63 mmol) in toluene (30 mL) was added an ethanolic solution (10 mL) of 3-isopropyl-phenylboronic acid (1.8 g, 11.28 mmol) followed by water (10 mL) and potassium carbonate (2.76 g, 20.0 mmol). The resulting mixture was degassed for 15 min (by purging with argon). At this time, Pd(PPh3)4 (0.613 g, 0.53 mmol) was added under argon and the reaction mixture was heated at 80° C. for 4 h. The reaction mixture was then cooled to room temperature and extracted with ethyl acetate (3×10 mL). The combined organic layers were washed with water (2×10 mL), dried over Na2SO4 and concentrated in vacuo to obtain the crude product, which was purified over silica gel (Biotage column chromatography, 2% ethyl acetate in hexane) to afford 0.900 g (59%) of 2-chloro-5-(3-isopropyl-phenyl)-pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263656B2
Source datasetuspto-grants-2012_09
ORD IDord-0acc0025e9e5431c82941bc424266945
Source noteuspto-grants-2012_09