HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906129Generated: October 29, 2026
Methyl iodide → Methyl 2-methyl-4-(methylamino)-3-nitrobenzoate
https://huagongshe.com/reaction/906129
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 67404328 | HCID 67404328 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 2-methyl-4-(methylamino)-3-nitrobenzoate | HCID 67403462 | 72.3% |
Reaction Steps
Iodomethane (125 uL, 2.0 mmol) was added to a mixture of the methyl 4-amino-2-methyl-3-nitrobenzoate (400 mg, 1.9 mmol) and sodium hydride (60% oil dispersion, 84 mg, 2.1 mmol) in tetrahydrofuran (10 mL) at 0° C. The reaction mixture was slowly warmed to room temperature and stirred for 18 hours. The reaction mixture was quenched with saturated aqueous ammonium chloride solution and extracted with ethyl acetate. The combined extract was washed with water (2×30 mL), brine (30 mL), dried over sodium sulfate, filtered and concentrated, then purified by flash chromatography (25% ethyl acetate in hexanes) to give methyl 2-methyl-4-(methylamino)-3-nitrobenzoate (308 mg, 72% yield). 1H NMR (400 MHz, CDCl3): 7.94 (d, 1H), 6.63 (d, 1H), 5.68 (br, 1H), 3.86 (d, 2H), 2.58 (s, 3H); MS (EI) for C10H12N2O4: 225 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08012956B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-c96b4f8d9d74455e93f6c16fffb51a11 |
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| Source note | uspto-grants-2011_09 |
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