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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604282Generated: October 29, 2026

Potassium methoxide → 3-Methoxy-2-methyl-6-nitro-benzoic acid

https://huagongshe.com/reaction/604282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium methoxideHCID 23664618—
Reactant3-Fluoro-2-methyl-6-nitrobenzoic acidHCID 50914948—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product3-Methoxy-2-methyl-6-nitro-benzoic acidHCID 59849216—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirring solution of 3-Fluoro-2-methyl-6-nitro-benzoic acid (4.2 g, 21 mmol) in THF (40 mL) and methanol (40 mL) is added potassium methoxide in methanol (15 g, 63 mmol) and the solution is heated to 100° C. for 2 hours. The reaction mixture is cooled to room temperature and then the mixture is quenched with a 1N HCl solution and partitioned between ethyl acetate. The organic layer is washed with brine and then concentrated to give 3-Methoxy-2-methyl-6-nitro-benzoic acid (4.3 g) in quantitative yields. 1H-NMR (400 MHz, δ, ppm) CDCl3: 2.32 (s, 3H), 3.98 (s, 3H), 6.95 (d, 1H), 8.15 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910585B2
Source datasetuspto-grants-2011_03
ORD IDord-3f209a146c5b445d80373c9e577888c9
Source noteuspto-grants-2011_03