戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 29028作成日:2026年10月23日

Nitrite → Nitroso acetamidophenol

https://huagongshe.com/ja/reaction/29028

反応式

関与物質

役割名称HCID仕込み量
反応物NitriteHCID 946—
反応物3-HydroxyacetanilideHCID 12124—
反応物Potassium nitriteHCID 516910—
反応物Sodium NitriteHCID 23668193—
生成物Nitroso acetamidophenolHCID 86605274—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07420054B2
出典データセットuspto-grants-2008_09
ORD IDord-520c41d065c54d5f8ad958d78d81c2b6
出典メモuspto-grants-2008_09