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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209705Generated: October 29, 2026

Hydroxyamine hydrochloride → N-hydroxy-2-[[4-hexyloxybenzenesulfonyl](isobutyl)amino]acetamide

https://huagongshe.com/reaction/2209705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodiumHCID 5360545—
ReactantEthyl 2-[[4-hexyloxybenzenesulfonyl](isobutyl)amino]acetateHCID 10834775—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
ProductN-hydroxy-2-[[4-hexyloxybenzenesulfonyl](isobutyl)amino]acetamideHCID 10738924—

Reaction Steps

Ethyl 2-[[4-hexyloxybenzenesulfonyl](isobutyl)amino]acetate (1.22 g, 3.05 mmol) is dissolved in methanol (15 mL). To this solution is added hydroxylamine hydrochloride (0.43 g, 6.11 mmol), followed by the addition of sodium methoxide, freshly prepared from sodium (0.35 g, 15.3 mmol) dissolved in methanol (5 mL). The reaction is stirred for 36 hours at room temperature. The reaction is worked up by partitioning between dilute hydrochloric acid (pH=~3) and ethyl acetate. The aqueous phase is extracted well with ethyl acetate, the combined organic layers are dried (Na2SO4), and the solvent is evaporated. The product is crystallized from hexane/ethyl acetate and collected by filtration to give N-hydroxy-2-[[4-hexyloxybenzenesulfonyl](isobutyl)amino]acetamide, m.p. 108°-110° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05455258
Source datasetuspto-grants-1995_10
ORD IDord-09c812c6836446b6865273c2cca496fc
Source noteuspto-grants-1995_10