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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1720615Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1720615

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 hexane/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
PatentnummerUS05506242
Quelldatensatzuspto-grants-1996_04
ORD IDord-26a5fd832430498eb795146c2cdef044
Quellennotizuspto-grants-1996_04