HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 742054Erstellt: 25. Oktober 2026
Hydroxyamine hydrochloride → N-hydroxy-2-[[4-hexyloxybenzenesulfonyl](isobutyl)amino]acetamide
https://huagongshe.com/reaction/742054
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydroxyamine hydrochloride | HCID 443297 | — |
| Edukt | Sodium | HCID 5360545 | — |
| Edukt | Ethyl 2-[[4-hexyloxybenzenesulfonyl](isobutyl)amino]acetate | HCID 10834775 | — |
| Edukt | Sodium Methoxide | HCID 10942334 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | N-hydroxy-2-[[4-hexyloxybenzenesulfonyl](isobutyl)amino]acetamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05552419 |
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| Quelldatensatz | uspto-grants-1996_09 |
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| ORD ID | ord-477f3476ce344ca290a646b1cb740e71 |
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| Quellennotiz | uspto-grants-1996_09 |
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