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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209677Generated: October 31, 2026

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

https://huagongshe.com/reaction/2209677

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 numberUS05455258
Source datasetuspto-grants-1995_10
ORD IDord-38e21aeeba7540168582deef9e506322
Source noteuspto-grants-1995_10