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HRID 36624Erstellt: 24. Oktober 2026

Sulfuric Acid → 7-Methyl-5-azaphenanthrene-1,10-dicarboxylic Anhydride

https://huagongshe.com/de/reaction/36624

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktNitrobenzeneHCID 7416—
EduktMethacrolein diacetateHCID 25305—
Edukt4-Aminonaphthalene-1,8-dicarboxylic anhydrideHCID 80990—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
Produkt7-Methyl-5-azaphenanthrene-1,10-dicarboxylic AnhydrideHCID 5437461793,7%

Reaktionsschritte

A mixture of 4-amino-1,8-naphthalic anhydride (Okazaki, M.; Ishikawa, N. Yuki Gosei Kagaku Kyokai Shi 1956, 14, 398; Chem. Abstr. 1957, 51, 8051c) (28.0 g, 131 mmol), ferrous sulfate heptahydrate (7.20 g, 25.8 mmol), concentrated sulfuric acid (13 mL, 234 mmol), and nitrobenzene (27.0 mL, 262 mmol) in acetic acid (260 mL) was heated to reflux. Methallylidene diacetate (43.5 mL, 262 mmol) was added dropwise over a period of 2.5 h using an addition funnel. After the addition was complete, the reaction mixture was heated for 1.5 h and poured into a beaker of ice/water (500 mL). The aqueous solution was further diluted to 800 mL with water, stirred for 1 h and filtered by suction. The residue was washed with water and dried in vacuo to obtain 32.3 g of a dark brown solid. The crude solid was heated at reflux in acetic acid (80 mL) and filtered hot to obtain 15.63 g (44%) of a light brown solid: mp >290° C.; MS m/e 264 (M+H+); 1H NMR (DMSO-d6, 300 MHz) δ 2.60 (s, 3H), 8.10 (t, 1H), 8.60 (s, 1H), 8.62 (s, 1H), 9.01 (s, 1H), 9.12 (d, 1H), 9.45 (d, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05416089
Quelldatensatzuspto-grants-1995_05
ORD IDord-e9d95a6fa62b41938daac5f7d4782911
Quellennotizuspto-grants-1995_05