HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113259Generated: October 27, 2026
Methanol → Methyl 4-amino-2,5-dimethylbenzoate
https://huagongshe.com/reaction/2113259
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Methyl 2,5-dimethyl-4-nitrobenzoate | HCID 57461068 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 4-amino-2,5-dimethylbenzoate | HCID 273299 | 100.4% |
Reaction Steps
To a stirred solution of methyl 2,5-dimethyl-4-nitrobenzoate (523 mg, 2.5 mmol) in a 9:1 mixture of methanol and water (25 mL total) at 0° C. was added ammonium chloride (401 mg, 7.5 mmol). Zinc (1.63 g, 25 mmol) was added portionwise and the resulting mixture was stirred at room temperature overnight. The reaction mixture was then filtered through Celite and the Celite pad was washed with methanol. The filtrate was concentrated under reduced pressure and the resulting residue was dissolved in ethyl acetate. This solution was washed with saturated aqueous sodium bicarbonate, dried over anhydrous sodium sulfate and concentrated under reduced pressure to provide methyl 4-amino-2,5-dimethylbenzoate (450 mg) as a yellow oil. 1H NMR (300 MHz, CDCl3) δ 2.14 (s, 3H), 2.53 (s, 3H), 3.83 (s, 3H), 3.85 (br s, 2H), 6.48 (s, 1H), 7.72 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07524965B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-56677d9e47984b6cbd4d15fa28c1edd7 |
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| Source note | uspto-grants-2009_04 |
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