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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098387Generated: November 1, 2026

Potassium Hydroxide → 4-Amino-N-hydroxy-2-methoxybenzamide

https://huagongshe.com/reaction/2098387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantMethyl 4-amino-o-anisateHCID 168705—
ReactantHydroxyamine hydrochlorideHCID 443297—
SolventMethanolHCID 887—
Product4-Amino-N-hydroxy-2-methoxybenzamideHCID 1604229347%

Reaction Steps

Methyl 2-methoxy-4-aminobenzoate (10 g, 55.25 mmol) and hydroxylamine hydrochloride (15.36 g, 221 mmol) were taken up in MeOH (80 ml) and a solution of KOH (15.4 g, 275 mmol) in MeOH (55 ml) was added carefully. The resultant mixture was stirred at reflux for 36 hrs. The volatiles were removed in vacuo The residue was taken up in 1M NaOH (50 ml) and washed with ethyl acetate (EtOAc, 50 ml). Concentrated HCl was added slowly until precipitation of a solid (pH was 10). The solid was filtered off, washed with H2O, then methyl-tert-butyl ether (MTBE) and dried under vacuum. 1H NMR showed the solid contained approx. 1/3 molar equivalent of ethyl acetate. The solid was taken up in 1M NaOH (100 ml) and the EtOAc was removed in vacuo. Concentrated HCl was added carefully until precipitation of a solid (pH was 8). The solid was collected by filtration, washed with H2O, then MTBE and dried under vacuum to give 4.67 g (47%) of the title compound as a dark red solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450506B2
Source datasetuspto-grants-2013_05
ORD IDord-931047eac5b4489cb82c7d0ec372e888
Source noteuspto-grants-2013_05