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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404728Generated: October 30, 2026

Benzyl Bromide → 1-Benzyloxy-6-bromo-isoquinoline

https://huagongshe.com/reaction/404728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactant6-Bromoisoquinolin-1(2H)-oneHCID 15885182—
CatalystHCID 178418647HCID 178418647—
SolventTolueneHCID 1140—
Product1-Benzyloxy-6-bromo-isoquinolineHCID 59226255—

Reaction Steps

To a solution of 3.93 g (17.5 mmol) 6-Bromo-2H-isoquinolin-1-one (6) in 150 ml Toluene were added 12.13 g (44.0 mmol) silver carbonate and 3.60 g (21.1 mmol) of benzyl bromide. The reaction mixture was refluxed for 1.5 h and then cooled to room temperature. The solution was filtered. The filtrate was washed with water and the aqueous phase extracted with ethyl acetate. The combined organic layers were dried over magnesium sulfate and evaporated. Final purification was achieved by preparative HPLC. Rt=2.47 min (Method B). Detected mass: 314.1/316.5 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748614B2
Source datasetuspto-grants-2014_06
ORD IDord-05fb1c7378b4455699fed5377735e176
Source noteuspto-grants-2014_06