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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913124Generated: October 31, 2026

Benzyl Bromide → 1-Benzyloxy-7-chloro-6-fluoro-isoquinoline

https://huagongshe.com/reaction/1913124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactant7-Chloro-6-fluoroisoquinolin-1(2H)-oneHCID 59818248—
CatalystHCID 178418647HCID 178418647—
SolventTolueneHCID 1140—
Product1-Benzyloxy-7-chloro-6-fluoro-isoquinolineHCID 5981825254.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

14.74 g (74.6 mmol) of 7-chloro-6-fluoro-2H-isoquinolin-1-one (101) were dissolved in 150 ml of toluene. After addition of 30.86 g (111.9 mmol) of silver carbonate and 15.31 g (89.5 mmol) of benzyl bromide, the mixture was stirred at 80° C. for 3 h. After cooling down to room temperature, the reaction mixture was filtered and the filtrate was evaporated. The residue was dissolved in dichloromethane and washed with water, dried with magnesium sulfate and evaporated. Final purification by preparative HPLC gave 11.63 g of the title compound. Rt=2.51 min (Method B). Detected mass: 288.1/290.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609691B2
Source datasetuspto-grants-2013_12
ORD IDord-da9b4eaa363a4de7917dfc8b6cee24f9
Source noteuspto-grants-2013_12