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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 8710Erstellt: 23. Oktober 2026

Isoquinoline → 5-Bromoisoquinoline

https://huagongshe.com/de/reaction/8710

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsoquinolineHCID 8405—
EduktSodium aluminateHCID 14766—
EduktSodium HydroxideHCID 14798—
EduktBromineHCID 24408—
EduktAluminumHCID 5359268—
EduktAluminum(III) ChlorideHCID 6451240—
Produkt5-BromoisoquinolineHCID 73648726%

Reaktionsbedingungen

Temperatur75 °C

Reaktionsschritte

The apparatus was a 500 mL three-necked flask equipped with a condenser, dropping funnel, and a stirrer terminating in a stiff, crescent-shaped Teflon polytetrafluroethylene paddle. To the isoquinoline (57.6 g, 447 mmol) in the flask was added AlCl3 (123 g, 920 mmol). The mixture was heated to 75–85° C. Bromine (48.0 g, 300 mmol) was added using a dropping funnel over a period of 4 hours. The resulting mixture was stirred for one hour at 75° C. The almost black mixture was poured into vigorously hand-stirred cracked ice. The cold mixture was treated with sodium hydroxide solution (10 N) to dissolve all the aluminum salts as sodium aluminate and the oily layer was extracted with ether. After being dried with Na2SO4 and concentrated, the ether extract was distilled at about 0.3 mm. A white solid (16.3 g, 78 mmol) from a fraction of about 125° C. was obtained (26% yield). The product was further purified by recrystallization (pentane or hexanes): mp 80–81° C.;

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07091212B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-b9469d6f4a4846c6b2874fbf0254c2dd
Quellennotizuspto-grants-2006_08