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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176849Generated: October 30, 2026

Sodium hydride → HCID 59287327, compound

https://huagongshe.com/reaction/2176849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2,3-Dimethyl-4-nitropyridine-N-oxideHCID 148223—
Reactant4-Bromo-3-fluorophenolHCID 2779153—
SolventDimethylformamideHCID 6228—
ProductHCID 59287327HCID 59287327175.5%

Reaction Conditions

Temperature180 °C

Reaction Steps

To a room temperature solution of 4-bromo-3-fluorophenol (15 g, 78.53 mmol) in DMF (50 ml) was added sodium hydride (3.32 g, 85.67 mmol, 60% in mineral oil) portionwise. After stirring for 10 minutes 2,3-dimethyl-4-nitro-pyridine 1-oxide (1.05 g, 6.28 mmol) was added The reaction mixture was heated at 180° C. for 60 minutes under microwave irradiation. After cooling to room temperature the mixture was filtered through a diatomaceous earth pad and the filtrate was then diluted with EtOAc and washed with water. The solution was then extracted with additional EtOAc (2×150 ml). The organic layer was dried (Na2SO4) and the solvent evaporated in vacuo. The crude product was purified by column chromatography (silica gel; DCM to DCM/MeOH up to 5% as eluent). The desired fractions were collected and evaporated in vacuo to yield intermediate 21 (3.44 g, 19%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067891B2
Source datasetuspto-grants-2015_06
ORD IDord-01ed3c7910e94c038feadd0092acfb89
Source noteuspto-grants-2015_06