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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878634Generated: October 26, 2026

Cesium carbonate → 2-Butyl-5-(4-phenylpyridin-3-yloxy)isoindolin-1-one

https://huagongshe.com/reaction/1878634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant2,2,6,6-Tetramethyl-3,5-heptanedioneHCID 70700—
Reactant3-Bromo-4-phenylpyridineHCID 2762928—
Reactant2-Butyl-5-hydroxyisoindolin-1-oneHCID 13897384—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product2-Butyl-5-(4-phenylpyridin-3-yloxy)isoindolin-1-oneHCID 5347724421%

Reaction Conditions

Temperature220 °C

Reaction Steps

A mixture of 3-bromo-4-phenylpyridine (50 mg, 0.213 mmol), 2-butyl-5-hydroxy-isoindolin-1-one (88 mg, 0.427 mmol), Cs2CO3 (139 mg, 0.427 mmol), CuI (16.3 mg, 0.085 mmol) and 2,2,6,6-tetramethyl-3.5-heptanedione (53 μL, 0.256 mmol) in degassed N-methylpyrrolidone (NMP) (2 mL) was stirred and heated in the microwave (220° C., 300 W, 30 min). Two of those reactions were combined, excess water and ethyl acetate were added. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The combined organic layers were extracted with aqueous HCl (2 M) and the combined extracts were basified with aqueous NaOH (2 M) followed by extraction with ethyl acetate. The combined organic layers were washed with water and dried over MgSO4. Purification by HPLC provided 2-butyl-5-(4-phenylpyridin-3-yloxy)isoindolin-1-one (16 mg, 8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314120B2
Source datasetuspto-grants-2012_11
ORD IDord-1db14dfe5fcf4e5595c7e889eae89bac
Source noteuspto-grants-2012_11