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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 5-amino-4-cyano-2-methylbenzoateHCID 67402842—
SolventDimethyl SulfoxideHCID 679—
ProductMethyl 5-amino-4-(aminocarbonyl)-2-methylbenzoateHCID 67403771208%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012956B2
Source datasetuspto-grants-2011_09
ORD IDord-681ce2a519fd405591d2cd681d47038d
Source noteuspto-grants-2011_09