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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium methoxide | HCID 23664618 | — |
| Reactant | 3-Fluoro-2-methyl-6-nitrobenzoic acid | HCID 50914948 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Methoxy-2-methyl-6-nitro-benzoic acid | HCID 59849216 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07910585B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-3f209a146c5b445d80373c9e577888c9 |
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| Source note | uspto-grants-2011_03 |
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