Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2306895Erstellt: 26. Oktober 2026

Quinizarin → 1,4-Anthraquinone

https://huagongshe.com/reaction/2306895

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktQuinizarinHCID 6688—
Edukt1,4-DimethoxyanthraceneHCID 83107—
EduktSodium borohydrideHCID 4311764—
LösungsmittelMethanolHCID 887—
LösungsmittelDiglymeHCID 8150—
Produkt1,4-AnthraquinoneHCID 6945795%

Reaktionsschritte

Although the preparation of 1,4-dimethoxyanthracene (1) has been reported (Criswell, et al., J. Org. Chem. 1974, 39, 770-774) by using methylation of quinizarin (3) followed by sequential reduction of the diketo function with sodium borohydride in diglyme, the difficulty in the reduction steps prompted us to investigate an easier method in the preparation of 1. Reduction of 3 with sodium borohydride in MeOH followed by quenching with HCl gave a 95% yield of 1,4-anthraquinone (4) (Scheme 2). Reduction of the quinone moiety of 4 with aqueous sodium hydrosulfite in 1,4-dioxane provided 1,4-dihydroxyanthracene (5). Methylation of 5 with sodium hydride in DMF at room temperature gave excellent yield of 1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06828450B2
Quelldatensatzuspto-grants-2004_12
ORD IDord-2846e1f06cac499386558423024d60af
Quellennotizuspto-grants-2004_12