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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037622Generated: October 27, 2026

Phenethyl bromide → HCID 66732112, compound

https://huagongshe.com/reaction/1037622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethyl bromideHCID 7666—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178517616HCID 178517616—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTolueneHCID 1140—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 66732112HCID 6673211277.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

7-Bromo-1-hydroxyisoquinoline (300 mg, 1.34 mmol, 1.0 equiv), tetrabutylammonium bromide (50 mg, 0.13 mmol, 0.10 equiv), and phenethyl bromide (220 uL, 1.6 mmol, 1.2 equiv) were combined in toluene (14 mL) and treated with 50% aq. NaOH (3 mL), and the resulting mixture stirred rapidly while heating to 80° C. After 1.5 hours, the mixture was diluted with MTBE and washed with water, saturated NaHCO3, and brine. The organic phase was dried over Na2SO4. Addition of silica gel, concentration, and purification of the crude residue using flash silica gel chromatography (gradient of 2-30% ethyl acetates/hexanes) provided 7-bromo-2-phenethyl-isoquinolin-1-one (340 mg, 1.04 mmol, 77%) as a white solid. This isoquinolinone (340 mg, 1.04 mmol) was converted, via Methods 1 and 2, to compound 11 (141 mg, 46%) which was isolated as a white solid. Activity: B

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546564B2
Source datasetuspto-grants-2013_10
ORD IDord-c088a60b2fd444428b957c31bf8c3d9a
Source noteuspto-grants-2013_10