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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493503Generated: October 31, 2026

Potassium Carbonate → HCID 86744826, compound

https://huagongshe.com/reaction/1493503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-Phenoxybenzyl chlorideHCID 93291—
ReactantHCID 15678649HCID 15678649—
CatalystTetrabutylammonium IodideHCID 67553—
SolventAcetonitrileHCID 6342—
ProductHCID 86744826HCID 8674482674.6%

Reaction Steps

A mixture of 2-[(2,6-dichlorophenyl)amino]-5-hydroxy benzene acetic acid methyl ester (2.5 g, 7.67 mmol) of Example 2F, powdered anhydrous potassium carbonate (0.55 g, 4 mmol), tetrabutylammonium iodide (0.050 g) and dry acetonitrile (50 mL) is stirred at room temperature under nitrogen for 30 min. To the slurry is then added 3-phenoxybenzylchloride (2 g, 9.17 mmol) and the mixture is placed in an oil bath maintained at 65°-70° C. overnight. The solvent is removed and the residue partitioned between water and ethyl acetate (50 mL each). The organic phase is washed with brine and dried (Na2SO4). The solvent is evaporated and the residue (brown oil, 4.2 g) is purified by flash chromatography (on silica Merck 60, hexane-ethyl acetate 85:15) to give the title product (yellow oil, 2.83 g, 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05021576
Source datasetuspto-grants-1991_06
ORD IDord-c273184d4c93491895d68d38db3b16af
Source noteuspto-grants-1991_06