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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 924408Generated: November 1, 2026

Sodium Carbonate → 3-(3-Nitropyridin-4-yl)cyclohex-2-enone

https://huagongshe.com/reaction/924408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Chloro-3-nitropyridineHCID 2735781—
Reactant3-(Tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohex-2-en-1-oneHCID 57496422—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
Product3-(3-Nitropyridin-4-yl)cyclohex-2-enoneHCID 5922654487%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohex-2-en-1-one (6.0 g, 27 mmol) and 4-chloro-3-nitropyridine (2.4 g, 15 mmol) in 1,4-dioxane (60 mL), 2.0 N aq. Na2CO3 (12 mL, 24 mmol) and tetrakis(triphenylphosphine)palladium(0) (1.8 g, 1.5 mmol) were added. The reaction mixture was heated at 120° C. for 1 h. The reaction mixture was filtered through diatomaceous earth, which was washed with EtOAc. The filtrate was concentrated under reduced pressure and the residue was purified by silica gel column chromatography (eluting with 10-100% EtOAc in hexanes) to give the sub-title compound as a brown solid (1.97 g, 87%). LCMS calc. for C11H11N2O3 (M+H)+: m/z=219.1. Found: 219.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278950B2
Source datasetuspto-grants-2016_03
ORD IDord-4416c30fbbca45078ff7baece52e298a
Source noteuspto-grants-2016_03