HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1469154Generated: October 31, 2026
Ammonium Chloride → Methyl 3-Amino-5-bromo-2-methylbenzoate
https://huagongshe.com/reaction/1469154
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Methyl 5-bromo-2-methyl-3-nitrobenzoate | HCID 24727998 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Methyl 3-Amino-5-bromo-2-methylbenzoate | HCID 24729181 | 99% |
Reaction Steps
To a stirred solution of methyl 5-bromo-2-methyl-3-nitrobenzoate (7.60 g, 27.7 mmol) in aq. EtOH (100 mL of EtOH and 20 mL of H2O) was added ammonium chloride (4.45 g, 83.1 mmol) and iron (4.64 g, 83.1 mmol). The reaction mixture was stirred at 80° C. for 5 hours. Then the mixture was filtered through Celite and the Celite bed was washed with ethyl acetate. The combined filtrate was concentrated in vacuo. The resultant residue was dissolved in ethyl acetate and water. The aqueous layer was extracted with ethyl acetate (twice). The combined organic layer dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to afford the titled compound as a brown oil (6.67 g, 99%). 1H-NMR (400 MHz, CDCl3) δ ppm; 7.37 (s, 1H), 6.92 (s, 1H), 3.94 (s, 3H), 3.80 (brs, 2H), 2.31 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09006242B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-49df4f83a0944e34abfd478f8722e593 |
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| Source note | uspto-grants-2015_04 |
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