Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | p-Nitrophenylacetonitrile | HCID 68386 | — |
| Edukt | Hydroxyamine hydrochloride | HCID 443297 | — |
| Edukt | Sodium methanolate methanol | HCID 23694274 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Produkt | N-hydroxy-2-(4-nitrophenyl)acetamidine | HCID 308292 | 59% |
Reaktionsschritte
To a mixture of hydroxylamine hydrochloride (21.5 g) and dimethyl sulfoxide (50 mL) was added dropwise 28% sodium methoxide methanol solution (59.6 g) at room temperature. A solution (50 mL) of (4-nitrophenyl)acetonitrile (10.0 g) in dimethyl sulfoxide was further added dropwise to the reaction mixture. The reaction mixture was stirred at 100° C. for 3 hrs. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated to give N′-hydroxy-2-(4-nitrophenyl)ethanimidamide as brown crystals (7.10 g, yield 59%). Recrystallization thereof from ethyl acetate-diisopropyl ether gave brown prism crystals. melting point: 170-171° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07423159B2 |
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| Quelldatensatz | uspto-grants-2008_09 |
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| ORD ID | ord-05d8c6aef45e47969bcddacab17cb55b |
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| Quellennotiz | uspto-grants-2008_09 |
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