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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 444661Erstellt: 26. Oktober 2026

Hydrochloric Acid → 3,7-Dibromodibenzo(b,d)thiophene

https://huagongshe.com/reaction/444661

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktDiethyl EtherHCID 3283—
Edukt3,7-Dibromo-dibenzothiophene 5,5-dioxideHCID 4071898—
EduktAluminium lithium hydrideHCID 21226445—
LösungsmittelWaterHCID 962—
LösungsmittelChloroformHCID 6212—
Produkt3,7-Dibromodibenzo(b,d)thiopheneHCID 80375948,1%

Reaktionsschritte

In a 500-ml flask, lithium aluminum hydride (4.1 g) is slowly introduced in small amounts over 50 minutes into a mixture of 3,7-dibromodibenzothiophene dioxide (20 g) and anhydrous ether (200 ml) in an ice bath, and the resulting mixture is refluxed and stirred for 2 hours. Water (200 ml) is added thereto to deactivate lithium aluminum hydride. Chloroform (200 ml) and concentrated hydrochloric acid (40 ml) are added thereto, the mixture is thoroughly stirred, and the organic layer is separated. The aqueous layer is further extracted with chloroform (200 ml×2), the chloroform extract is combined with the organic layer, and the combined organic layer is washed with water (200 ml) and saturated brine (200 ml), and dried over calcium chloride. The solvent is distilled off, and colorless crystals thus obtained are recrystallized from ethyl acetate+ethanol (16:3). Thus, 8.8 g of 3,7-dibromodibenzothiophene is obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08475984B1
Quelldatensatzuspto-grants-2013_07
ORD IDord-e8993a482e264607916821b1a435b3a0
Quellennotizuspto-grants-2013_07