Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 493095Erstellt: 23. Oktober 2026

Benzofuran → 3-Bromo-1-benzofuran

https://huagongshe.com/de/reaction/493095

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzofuranHCID 9223—
EduktBromineHCID 24408—
Edukt2,3-Dibromo-2,3-dihydrobenzofuranHCID 12394037—
LösungsmittelEthanolHCID 702—
LösungsmittelChloroformHCID 6212—
Produkt3-Bromo-1-benzofuranHCID 64058990,2%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Bromine (13.1 mL, 250 mmol) dissolved in chloroform (50 mL) is added dropwise to a solution of benzo[b]furan (25 g, 210 mmol) in chloroform (200 mL) at −10° C. over 20 minutes. The mixture is then stirred at 0° C. for 1 hour and the volatiles are evaporated. The residue is stirred with ethanol (50 mL) and then filtered. The solid material is washed with diethyl ether (100 mL) on the filter. This furnishes 23.0 g (39%) of 2,3-dibromo-2,3-dihydro-benzo[b]furan as white crystalline material. Potassium hydroxide pellets (9.3 g, 165 mmol) are dissolved in ethanol (40 mL) and cooled to 0° C. 2,3-Dibromo-2,3-dihydro-benzo[b]furan (23.0 g, 82.7 mmol) dissolved in ethanol (90 mL) is added dropwise hereto at a constant temperature of 0° C. After complete addition the mixture is heated to reflux for 2 hours. The mixture is concentrated in vacuo and water (100 mL) is added. The aqueous layer is extracted with ethyl acetate (3×100 mL). The combined organic fractions are washed with brine (100 mL), dried (MgSO4) and concentrated to furnish 14.7g (90%) of the wanted product as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07534791B2
Quelldatensatzuspto-grants-2009_05
ORD IDord-b013d651b6574729a4f272e502124691
Quellennotizuspto-grants-2009_05