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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 42218Erstellt: 24. Oktober 2026

Ammonium Chloride → 1-Benzyl-4-bromoisoquinoline

https://huagongshe.com/de/reaction/42218

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
Edukt4-Bromo-1-chloroisoquinolineHCID 459766—
EduktHCID 178419772HCID 178419772—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-Benzyl-4-bromoisoquinolineHCID 2362841825%

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

In a 40 mL vial 490 mg (2.00 mmol) 1-chloro-4-bromo-isoquinoline and 40 mg (0.034 mmol) tetrakis(triphenylphosphine)palladium(0) is added to 4 mL THF. After all solids are dissolved, 8 mL of 0.5 M (4.0 mmol) benzyl zinc bromide in THF is slowly added by syringe and the resulting reaction mixture is stirred at 25° C. After 12 hrs, the mixture is poured into cold solution of saturated NH4Cl and extracted with EtOAc. The organic extracts are concentrated in vacuo and the resulting residue is purified by silica chromatography using a heptane/EtOAc gradient. Pure fractions are pooled and evaporated to give 150 mg (0.50 mmol) of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08536168B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-219230f852f44f51bfb10fb2f15a93bf
Quellennotizuspto-grants-2013_09