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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72267Generated: October 29, 2026

Potassium Phosphate, Tribasic → 3-[5-(5-Chloropyridin-2-yl)-2-ethylphenyl]bicyclo[3.2.1]octane-2,4-dione

https://huagongshe.com/reaction/72267

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Bromo-5-chloropyridineHCID 817098—
Reactant3-(2,4-Dioxobicyclo[3.2.1]oct-3-yl)-4-ethylphenylboronic acidHCID 68480644—
ReactantCID 86657037HCID 86657037—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetonitrile--water (1/1)HCID 18373917—
Product3-[5-(5-Chloropyridin-2-yl)-2-ethylphenyl]bicyclo[3.2.1]octane-2,4-dioneHCID 68486488—

Reaction Steps

To a microwave vial containing 3-(2,4-dioxobicyclo[3.2.1]oct-3-yl)-4-ethylphenylboronic acid (0.15 g, 0.52 mmol) and potassium phosphate (0.667 g, 3.15 mmol) is added 2-bromo-5-chloropyridine (0.121 g, 0.63 mmol), palladium acetate (4.0 mg, 0.016 mmol) and tris(3-sulfophenyl)phosphine trisodium salt (21 mg, 0.038 mmol). A degassed solvent mixture of water/acetonitrile (1.6 ml, 2:1 ratio) is then added, followed by flushing with nitrogen, then stirring at ambient temperature for 5 minutes before heating at 160° C. under microwave irradiation for 15 minutes. After cooling to room temperature the reaction is partitioned between 2M aqueous hydrochloric acid and dichloromethane, and the organic phase is separated. The aqueous phase is further extracted with dichloromethane and all organic fractions are combined then evaporated. The residue is purified by preparative reverse-phase HPLC to give 3-[5-(5-chloropyridin-2-yl)-2-ethylphenyl]bicyclo[3.2.1]octane-2,4-dione.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08828908B2
Source datasetuspto-grants-2014_09
ORD IDord-e85d6ce6ab204b93892985b05e1aa092
Source noteuspto-grants-2014_09