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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925936Generated: October 31, 2026

Phenol → Ethyl 5-amino-2-phenoxybenzoate

https://huagongshe.com/reaction/1925936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 2-fluoro-5-nitrobenzoateHCID 12793176—
SolventDimethylformamideHCID 6228—
ProductEthyl 5-amino-2-phenoxybenzoateHCID 5384824982.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of ethyl 2-fluoro-5-nitrobenzoate (1.07 g), phenol (565 mg), potassium carbonate (1.38 g) and N,N-dimethylformamide (20 mL) was stirred at 80° C. for 4 hrs. The reaction mixture was concentrated under reduced pressure. Water was added to the residue and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (eluent, ethyl acetate:hexane=20:80→30:70). The object fraction was concentrated under reduced pressure and ethanol (20 mL) and 10% palladium on carbon (1.5 g) were added to the residue (1.54 g). The mixture was stirred overnight under a hydrogen stream. The catalyst was filtered off, and the filtrate was concentrated. The obtained residue was purified by silica gel column chromatography (eluent, ethyl acetate:hexane=20:80→50:50) and recrystallized from diisopropyl ether-hexane to give the title compound (1.07 g) as a pale-brown powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178543B2
Source datasetuspto-grants-2012_05
ORD IDord-0d0579026d814624b809b1c009ca693a
Source noteuspto-grants-2012_05