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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 349055Erstellt: 24. Oktober 2026

7-Bromo-1-Chloroisoquinoline → 7-Bromo-1-butylisoquinoline

https://huagongshe.com/de/reaction/349055

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt7-Bromo-1-ChloroisoquinolineHCID 6502024—
EduktHCID 178418265HCID 178418265—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelEthyl AcetateHCID 8857—
Produkt7-Bromo-1-butylisoquinolineHCID 2108599524,4%

Reaktionsschritte

To a refluxing solution of 7-bromo-1-chloroisoquinoline (4.85 g, 23.28 mmol) in diethyl ether (75 mL) was added butylmagnesium chloride (17.8 mL, 2.0 M ether, 35.6 mmol) and the reaction maintained at reflux for 2 h. The reaction mixture was cooled to room temperature, carefully diluted with an equal volume of ethyl acetate, washed with saturated sodium bicarbonate, water, and saturated sodium chloride, dried (sodium sulfate), filtered, and concentrated under reduced pressure to give an brown oil. Purification by flash column chromatography (silica, 1–10% ether/hexanes) gave the desired 7-bromo-1-butylisoquinoline (1.50 g): ESI MS m/z 264 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07176242B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-08c206c12c7d441bac3b2682a3e116dc
Quellennotizuspto-grants-2007_02