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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742029Generated: October 30, 2026

Hydroxyamine hydrochloride → N-hydroxy-2-[[4-methoxybenzenesulfonyl](benzyl)amino]propionamide

https://huagongshe.com/reaction/742029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl 2-[[4-methoxybenzenesulfonyl](benzyl)amino]propionateHCID 22907154—
SolventMethanolHCID 887—
ProductN-hydroxy-2-[[4-methoxybenzenesulfonyl](benzyl)amino]propionamideHCID 15296597—

Reaction Steps

Methyl 2-[[4-methoxybenzenesulfonyl](benzyl)amino]propionate (2.1 g, 6.01 mmol) is dissolved in methanol (20.0 mL). To this solution is added hydroxylamine hydrochloride (0.84 g, 12.0 mmol), followed by the addition of sodium methoxide (7.0 mL of a 4.37M solution). The reaction is stirred overnight at room temperature. The reaction is worked up by first removing all the solvent, and partitioning between ethyl acetate/hexane (2/1) and saturated sodium bicarbonate. The aqueous phase is extracted well with ethyl acetate/hexane, the combined organic layers are dried (MgSO4), and the solvent is evaporated. The product is purified by silica gel chromatography (ethyl acetate) to give N-hydroxy-2-[[4-methoxybenzenesulfonyl](benzyl)amino]propionamide, m.p. 149°-151° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05552419
Source datasetuspto-grants-1996_09
ORD IDord-00b694a9bfee4a718c81ecbe5f01804f
Source noteuspto-grants-1996_09