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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618279Generated: November 2, 2026

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

https://huagongshe.com/reaction/1618279

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Bromo-4-hydroxy-isoquinoline-3-carboxylic acid butyl esterHCID 86014541—
SolventAcetoneHCID 180—
Product4-Benzyloxy-1-bromo-isoquinoline-3-carboxylic acid butyl esterHCID 86014503—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765956B2
Source datasetuspto-grants-2014_07
ORD IDord-87b9d99c8bcc444ca5724e0a709c25e4
Source noteuspto-grants-2014_07