Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Nitrite | HCID 946 | — |
| Edukt | 3-Hydroxyacetanilide | HCID 12124 | — |
| Edukt | Potassium nitrite | HCID 516910 | — |
| Edukt | Sodium Nitrite | HCID 23668193 | — |
| Produkt | Nitroso acetamidophenol | HCID 86605274 | — |
Reaktionsschritte
According to this scheme 1a, the compounds of formula (Ia) are prepared by reaction of an appropriate 3-acetamidophenol compound (1) with a nitrite (2), such as a sodium nitrite (X═Na), a potassium nitrite (X═K), etc., at a temperature of −3° C. The nitroso acetamidophenol (3) thus obtained is subsequently reacted with 1,3-dihydroxynaphthalene (4) in a solvent such as butanol, by heating to a temperature of approximately 70° C., then adding concentrated sulfuric acid and continuing the heating to 90° C., and then cooling, so as to form the appropriate 9-acetamido-benzo[a]phenoxazin-5-one. The latter compound is subsequently hydrolyzed by heating with moderately concentrated sulfuric acid so as to give the 9-amino-benzo[a]phenoxazin-5-one (5). The last step is equivalent to that of scheme 1.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07695930B2 |
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| Quelldatensatz | uspto-grants-2010_04 |
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| ORD ID | ord-a475a9d865ae42dbbce8b42d5588989d |
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| Quellennotiz | uspto-grants-2010_04 |
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