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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 250457Erstellt: 27. Oktober 2026

Benzyl Bromide → 4-Benzyloxy-1-bromo-isoquinoline-3-carboxylic acid butyl ester

https://huagongshe.com/reaction/250457

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
EduktPotassium CarbonateHCID 11430—
Edukt1-Bromo-4-hydroxy-isoquinoline-3-carboxylic acid butyl esterHCID 86014541—
LösungsmittelAcetoneHCID 180—
Produkt4-Benzyloxy-1-bromo-isoquinoline-3-carboxylic acid butyl esterHCID 86014503—

Reaktionsschritte

A mixture of 1-bromo-4-hydroxy-isoquinoline-3-carboxylic acid butyl ester (6.48 g, 20 mmol; Example D-28 a), benzyl bromide (3.6 ml, 30 mmol), K2CO3 (12.44 g, 90 mmol) and acetone (300 ml) was refluxed with stirring for 2.5 d. The solvent was then evaporated in vacuo. To the residue was added water (100 ml) and the mixture was extracted with EtOAc (100 ml). The organic phase was dried over MgSO4 and evaporated in vacuo to give the title compound as a yellowish solid; MS-(+)-ion: M+1=414.1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07863292B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-fc8d1a74afb84d69a3ef9241881514b9
Quellennotizuspto-grants-2011_01