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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 264319Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/264319

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydroxyamine hydrochlorideHCID 443297—
EduktSodiumHCID 5360545—
EduktEthyl 2-[[4-hexyloxybenzenesulfonyl](isobutyl)amino]acetateHCID 10834775—
EduktSodium MethoxideHCID 10942334—
LösungsmittelMethanolHCID 887—
ProduktN-hydroxy-2-[[4-hexyloxybenzenesulfonyl](isobutyl)amino]acetamideHCID 10738924—

Reaktionsschritte

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 hexnae/ethyl acetate and collected by filtration to give N-hydroxy-2-[[4-hexyloxybenzenesulfonyl](isobutyl)amino]acetamide, m.p. 108°-110° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05646167
Quelldatensatzuspto-grants-1997_07
ORD IDord-0b55bed1ad31402aa6efa71dcdffe34c
Quellennotizuspto-grants-1997_07