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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767613Generated: October 29, 2026

Sodium Hydroxide → 2-Amino-5-(1-hydroxyiminoethyl)benzenesulfonamide

https://huagongshe.com/reaction/1767613

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant5-Acetyl-2-aminobenzenesulfonamideHCID 12952399—
SolventEthanolHCID 702—
Product2-Amino-5-(1-hydroxyiminoethyl)benzenesulfonamideHCID 13011928581%

Reaction Steps

To a suspension of 5-acetyl-2-aminobenzenesulfonamide (see compound 13) (0.45 g, 2.1 mmol) in 96% EtOH (40 ml) was added H2NOH.HCl (0.28 g, 4 mmol) and 2M NaOH (2 ml). The mixture was boiled for 2 h and the solvent was evaporated. The residue was triturated with water (25 ml) and the product was filtered off and dried, yielding 0.39 g (81%) of 2-amino-5-(1-hydroxyiminoethyl)benzenesulfonamide as yellow powder. The product was further transformed by Method G (using cyclohexanecarboxaldehyde). M.p. 230–233° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235548B2
Source datasetuspto-grants-2007_06
ORD IDord-1d1c34e23e824dc0a31a5e8ca498eb5a
Source noteuspto-grants-2007_06