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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523803Generated: October 25, 2026

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

https://huagongshe.com/reaction/523803

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 numberUS09339527B2
Source datasetuspto-grants-2016_05
ORD IDord-4eb57ac5552243c4af373d2133096e2e
Source noteuspto-grants-2016_05