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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095804Generated: November 1, 2026

Sulfuric Acid → 1-(2-Bromo-4-fluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridine-3-carboxylic acid

https://huagongshe.com/reaction/2095804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
Reactant1-(2-Bromo-4-fluorophenyl)-4-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrileHCID 66968834—
ReactantHCID 66968998HCID 66968998—
SolventWaterHCID 962—
Product1-(2-Bromo-4-fluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridine-3-carboxylic acidHCID 6696855053%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a mixture of 1-(2-bromo-4-fluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile, 1-(2-bromo-4-fluorophenyl)-4-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile (2.00 g, 6.51 mmol) and water (10 mL) was added conc. sulfuric acid (10 mL) at 0° C., and the mixture was stirred at 100° C. for 16 hr. After cooling to 0° C., the mixture was basified (pH 11) with 8N aqueous sodium hydroxide solution and washed with ethyl acetate. The aqueous layer was acidified (pH 4) with 5N hydrochloric acid and extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and filtered, and the solvent was evaporated under reduced pressure. The obtained residue was washed with diethyl ether and collected by filtration to give the title compound (1.12 g, 53%) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445509B2
Source datasetuspto-grants-2013_05
ORD IDord-c29da9e682cf435ea19d2c0b2e3b5545
Source noteuspto-grants-2013_05