HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110012Generated: November 4, 2026
Methylamine → Methyl 4-(methylamino)-3-nitrobenzoate
https://huagongshe.com/reaction/2110012
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Methyl 4-fluoro-3-nitrobenzoate | HCID 5219721 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 4-(methylamino)-3-nitrobenzoate | HCID 7650848 | — |
Reaction Steps
After dissolving 4-fluoro-3-nitrobenzoic acid methyl ester (507.3 mg, 2.55 mmol) in tetrahydrofuran (1 ml), methylamine (2.0 M tetrahydrofuran solution, 2.55 ml, 5.09 mmol) was added in an ice bath, and the mixture was stirred at room temperature overnight; The reaction mixture was concentrated under reduced pressure and dissolved in ethyl acetate (20 ml), and after washing in saturated aqueous sodium bicarbonate and brine, it was dried over anhydrous magnesium sulfate. It was then concentrated under reduced pressure, the obtained residue was dissolved in a methylamine-tetrahydrofuran solution (2.0 M, 3 ml), and upon sealing, the solution was stirred at 50° C. for 5 hours. The reaction mixture was concentrated under reduced pressure and dissolved in ethyl acetate (30 ml), and the solution was washed with saturated aqueous sodium bicarbonate and brine and then dried over anhydrous magnesium sulfate. The dried product was concentrated under reduced pressure to obtain 4-methylamino-3-nitro-benzoic acid methyl ester. The compound was identified by LC-MS.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07517875B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-1af70feea21f4c1b8b2c2c71b721431c |
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| Source note | uspto-grants-2009_04 |
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