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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115768Generated: November 1, 2026

Thiophenol → HCID 67520293, compound

https://huagongshe.com/reaction/2115768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
ReactantPotassium HydroxideHCID 14797—
Reactant4-Chloro-6,7-dimethoxyquinolineHCID 459610—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 67520293HCID 67520293—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 4-chloro-6,7-dimethoxy-quinoline (214 mg, 0.96 mmol) in EtOH (10 mL) and H2O (10 mL), was added KOH (107 mg, 1.44 mmol). The solution was stirred in a 100° C. bath. Then thiophenol (148 μL, 1.44 mmol) was added. The reaction was stirred at 100° C. for 1 h. The solvent was removed by rotary evaporation. The resulting residue was worked up with water and extracted with EtOAc 3×. The combined organic layer was washed with water and brine, dried over Na2SO4, filtered, and concentrated in vacuo. The crude material was purified by silica gel prep-TLC with 100% EtOAc to give the titled compound. MS (ESI, pos. ion) m/z: 298.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435823B2
Source datasetuspto-grants-2008_10
ORD IDord-53522052beea40f4950521efc64e52b1
Source noteuspto-grants-2008_10