HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906181Generated: November 1, 2026
Hydrogen Peroxide → Methyl 5-amino-4-(aminocarbonyl)-2-methylbenzoate
https://huagongshe.com/reaction/906181
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 5-amino-4-cyano-2-methylbenzoate | HCID 67402842 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | Methyl 5-amino-4-(aminocarbonyl)-2-methylbenzoate | HCID 67403771 | 208% |
Reaction Steps
Methyl 5-amino-4-cyano-2-methylbenzoate (151 mg, 0.79 mmol) (synthesized according to reagent preparation 41) was dissolved in DMSO (1.5 mL). 30% Aqueous hydrogen peroxide (0.3 mL) and potassium carbonate (35 mg, 0.25 mmol) were added, and the mixture was stirred at ambient temperature for 1.5 h. The reaction mixture was partitioned between ethyl acetate and water. The aqueous portion was extracted (2×) with ethyl acetate. The combined organic portion was dried over sodium sulfate, filtered and concentrated to a yellow oil which was purified by preparative reverse phase HPLC to afford methyl 5-amino-4-(aminocarbonyl)-2-methylbenzoate (108 mg, 0.52 mmol, 66% yield). NMR (400 MHz, CDCl3): δ 7.85 (s, 1H), 7.45 (br s, 1H), 7.26 (s, 1H), 7.19 (br s, 1H), 6.48 (s, 2H), 3.80 (s, 3H), 2.32 (s, 3H); MS (EI) for C10H12N2O3: 209 (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-681ce2a519fd405591d2cd681d47038d |
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| Source note | uspto-grants-2011_09 |
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