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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 525979Erstellt: 23. Oktober 2026

Quinizarin → 1,4-Bis(octyloxy)anthracene-9,10-dione

https://huagongshe.com/de/reaction/525979

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktQuinizarinHCID 6688—
Edukt1-BromooctaneHCID 8140—
EduktPotassium CarbonateHCID 11430—
LösungsmittelDimethylformamideHCID 6228—
Produkt1,4-Bis(octyloxy)anthracene-9,10-dioneHCID 6844131737,7%

Reaktionsschritte

1,4-dihydroxyanthracene-9,10-dione (5.0 g, 20.6 mmol), 1-bromooctane (10.0 g, 51.8 mmol), and potassium carbonate (37 g, 0.268 mol) was mixed in N,N-dimethylformamide and heated at 90° C. for 7 h after which the potassium carbonate was filtered off. The reaction mixture was quenched with water and extracted three times with ether. The ether was then washed three times with 1M HCl, one time with water, and evaporated to give a dark yellow solid. This solid was recrystallised in methanol to yield 1,4-bis(octyloxy)anthracene-9,10-dione (1.81 g, 3.88 mmol) as a yellow solid. 1H-NMR (CDCl3, δ): 0.89 (t, 6H), 1.2-1.4 (m, 16H), 1.53 (m, 4H), 1.93 (m, 4H), 4.10 (t, 4H), 7.30 (s, 2H), 7.71 (m, 2H), 8.16 (m, 2H) MS MALDI-TOF (m/z): 464.328

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09343198B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-555a9ae8fe2840619383765dd74b0a95
Quellennotizuspto-grants-2016_05