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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 256272Erstellt: 25. Oktober 2026

Acetic Acid → 1,4-Bis(p-octyloxybenzylidene amino)anthraquinone

https://huagongshe.com/reaction/256272

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktDisperse Violet 1HCID 31420—
Eduktp-(Octyloxy)benzaldehydeHCID 90358—
LösungsmittelMethanolHCID 887—
Produkt1,4-Bis(p-octyloxybenzylidene amino)anthraquinoneHCID 20163337—

Reaktionsschritte

In a round-bottomed flask fitted with thermometer, reflux condenser and stirrer is placed a mixture of 25 ml. glacial acetic acid and 50 ml methanol and in it is dissolved 2.38 g (0.1 mol) 1,4-diaminoanthraquinone. There is taken added 4.68 g (0.2 mol) p-octyloxybenzaldehyde and the mixture is heated at 90° for one hour. The reaction mixture is cooled to about 20°-25° and poured into ice water. The precipitated product is collected and recrystallized from ethylene glycol monomethyl ether or 1:1 methanol water as small purple needles. The crystallization is repeated twice more to obtain 1,4-bis(p-octyloxybenzylidene amino)anthraquinone m.p. 280° C. (dec) having absorption spectra in visual and infra red ranges as shown in FIGS. 9, 10, and 11 and of sufficient purity for use in guest-host combinations.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04702561
Quelldatensatzuspto-grants-1987_10
ORD IDord-65f3fe035b924f5591f1558c0da1310b
Quellennotizuspto-grants-1987_10