HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 238930Erstellt: 24. Oktober 2026
Hydroxyamine hydrochloride → N-{4-[1-(hydroxyamino)ethylidene]cyclohexa-2,5-dien-1-ylidene}methanesulfonamide
https://huagongshe.com/de/reaction/238930
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydroxyamine hydrochloride | HCID 443297 | — |
| Edukt | N-(4-acetylphenyl)methanesulfonamide | HCID 684083 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | N-{4-[1-(hydroxyamino)ethylidene]cyclohexa-2,5-dien-1-ylidene}methanesulfonamide | HCID 6612326 | — |
Reaktionsschritte
A mixture of 4′-(Methylsulfonylamino)acetophenone (13-5, 5 mmol) and hydroxylamine hydrochloride (0.695 g, 10 mmol) in pyridine (5 mL) was heated at 70° C. for 3 h. The reaction mixture was cooled to room temperature, diluted with H2O, and extracted with EtOAc several times. The combined organic layers were washed with H2O and brine, dried over MgSO4, filtered, and the filtrate was concentrated in vacuo. The residue was purified by flash column chromatography on silica gel using EtOAc:hexanes (1:1) as eluant to 4′-Methylsulfonylamino)acetophenone oxime (13-8, LJO-299).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08642657B2 |
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| Quelldatensatz | uspto-grants-2014_02 |
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| ORD ID | ord-8be3c1feb80d41cca7259ae6441eb595 |
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| Quellennotiz | uspto-grants-2014_02 |
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