Quinizarin → 1,4-Anthraquinone

HRID 2306895

Reaktionsgleichung

Reaktionsgleichung von HRID 2306895
C[O:2][C:3]1[C:16]2[C:7](=[CH:8][C:9]3[C:14]([CH:15]=2)=[CH:13][CH:12]=[CH:11][CH:10]=3)[C:6]([O:17]C)=[CH:5][CH:4]=1.C1C=CC2C(=O)C3C(=C(O)C=CC=3O)C(=O)C=2C=1.[BH4-].[Na+]>COCCOCCOC.CO>[C:3]1(=[O:2])[C:16]2[C:7](=[CH:8][C:9]3[C:14]([CH:15]=2)=[CH:13][CH:12]=[CH:11][CH:10]=3)[C:6](=[O:17])[CH:5]=[CH:4]1

Komponenten

6

Edukt 3

HCID 6688QuinizarinHCID 831071,4-DimethoxyanthraceneHCID 4311764Sodium borohydride2×

Produkt 1

HCID 694571,4-AnthraquinoneAusbeute 95 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 887MethanolLösungsmittelHCID 8150DiglymeLösungsmittel

Versuchsvorschrift

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.

Aufarbeitung

  1. customin the preparation of 1
  2. customby quenching with HCl

Quellen und Nachweise

ORD-Eintrag
ord-2846e1f06cac499386558423024d60af
Quelldatensatz
uspto-grants-2004_12
Patentnummer
US06828450B2

Verknüpfte Notizen

Wird geladen…