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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388068Generated: October 25, 2026

Ethyl Acetate → 4-(4-Amino-2,3-dimethylphenoxy)-7-benzyloxy-6-cyanoquinoline

https://huagongshe.com/reaction/388068

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactant4-HydroxyxylidineHCID 76542—
Reactant7-Benzyloxy-4-chloro-6-cyanoquinolineHCID 22646519—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product4-(4-Amino-2,3-dimethylphenoxy)-7-benzyloxy-6-cyanoquinolineHCID 2293651642.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

4-Amino-2,3-xylenol (2.80 g) purchased from Tokyo Chemical Industries was dissolved in dimethylsulfoxide (15 ml), and after gradually adding sodium hydride (816 mg) at room temperature, the mixture was stirred for 20 minutes. 7-Benzyloxy-4-chloro-6-cyanoquinoline (3.0 g) was added, and the mixture was heated at 100° C. for 4 hours while stirring. After cooling to room temperature, the reaction solution was distributed between ethyl acetate and water, and the organic layer was washed with water, 1N aqueous sodium hydroxide and saturated saline and dried over anhydrous sodium sulfate. The solvent was distilled off, and the obtained crude product was washed with ethyl acetate to obtain the title compound (1.72 g) as light brown crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372981B2
Source datasetuspto-grants-2013_02
ORD IDord-a5b9a3d025b349dc83b7d96b0902e1fd
Source noteuspto-grants-2013_02