HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2208731Generated: November 2, 2026
Methyl iodide → Methyl 5-bromo-2-methyl-3-nitrobenzoate
https://huagongshe.com/reaction/2208731
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 5-Bromo-2-methyl-3-nitrobenzoic acid | HCID 13770008 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 5-bromo-2-methyl-3-nitrobenzoate | HCID 24727998 | 94.9% |
Reaction Steps
To a stirred solution of 5-bromo-2-methyl-3-nitrobenzoic acid (16 g, 61.54 mmol) in DMF (160 mL), iodomethane (35.72 g, 248 mmol) and sodium carbonate (26.28 g, 248 mmol) were added. Resulting reaction mass was stirred at 60° C. for 8 h. On completion, reaction mass was filtered and inorganic solid residue washed with ethyl acetate. Combined filtrate was concentrated under vacuum till dryness. The residue was re-dissolved in ethyl acetate and washed with 5% sodium bicarbonate solution (700 mL) followed by 5M HCl solution (300 mL). Organic layer was finally washed with brine, dried over sodium sulfate, filtered and concentrated to afford the desired compound (16 g. 94.50%).
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-6cb273f47f744aa6b0c9ac071d544440 |
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| Source note | uspto-grants-2016_06 |
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