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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2405779Generated: October 25, 2026

3-Chloroisoquinoline → 3-Ethoxyisoquinoline

https://huagongshe.com/reaction/2405779

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-ChloroisoquinolineHCID 640968—
ReactantPotassium ethoxideHCID 23670592—
Product3-EthoxyisoquinolineHCID 64096648.1%

Reaction Conditions

Temperature150 °C

Reaction Steps

3-Chloroisoquinoline (3.0, 18 mmol) was dissolved in potassium ethoxide (24% in EtOH, 10.6 mL, 27 mmol) and heated to 150° C. in a sealed tube for 24 h. After cooling, the solvent was removed in vacuo and the residue treated with 1M HCl until the solution reaches a pH 3. Saturated NaHCO3 solution then added slowly to return the solution to pH 8 followed by extraction with CHCl3. The combined organics were washed with brine, dried over anhydrous MgSO4. The residue obtained from concentration in vacuo was purified by column chromatography on SiO2 (0-15% EtOAc, hex) to afford 1.5 g (48%) of 3-ethoxyisoquinoline. LCMS found 174.11 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809267B2
Source datasetuspto-grants-2014_08
ORD IDord-cef4d907a0fd4ddcb31109763f85a618
Source noteuspto-grants-2014_08