HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2208661Generated: November 3, 2026
Methyl iodide → Methyl 2-methyl-3-nitro-5-(trifluoromethyl)benzoate
https://huagongshe.com/reaction/2208661
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Methyl-3-nitro-5-(trifluoromethyl)benzoic acid | HCID 68295501 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-methyl-3-nitro-5-(trifluoromethyl)benzoate | HCID 68295416 | 90.2% |
Reaction Steps
To a solution of 2-methyl-3-nitro-5-(trifluoromethyl)benzoic acid (21.0 g, 84.3 mmol) in DMF (200 mL) was added potassium carbonate (35.0 g, 253 mmol) and methyl iodide (24.0 g, 169 mmol). The mixture was stirred at 60° C. and after stirring for 6 h the reaction mixture was cooled to 23° C. and was filtered. The filtrate was concentrated in vacuo and the residue was dissolved in EtOAc and water. The aqueous phase was extracted with EtOAc (2×250 mL and the combined organic layers were concentrated in vacuo. The residue was purified by column chromatography (SiO2 heptane-EtOac=4/1) to give the titled compound (20.0 g, 90% yield). 1H-NMR (400 MHz, CDCl3) δ (ppm); 8.27 (s, 1H), 8.11 (s, 1H), 3.99 (s, 3H), 2.71 (s, 3H); MS (ES) [M−H] 261.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09376422B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-4fc0f9fad0d44f32b7035955d42d1084 |
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| Source note | uspto-grants-2016_06 |
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