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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78316Generated: October 25, 2026

Water → Ethyl 3-(4-nitrophenoxy)benzoate

https://huagongshe.com/reaction/78316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 3-hydroxybenzoateHCID 24522—
SolventDimethylformamideHCID 6228—
ProductEthyl 3-(4-nitrophenoxy)benzoateHCID 1132365488.2%

Reaction Steps

A mixture of 4-fluoro-1-nitrobenzene (16 mL, 150 mmol), ethyl 3-hydroxybenzoate 25 g, 150 mmol) and K2CO3 (41 g, 300 mmol) in DMF (125 mL) was heated at the reflux temp. overnight, cooled to room temp. and treated with water (250 mL). The resulting mixture was extracted with EtOAc (3×150 mL). The combined organic phases were sequentially washed with water (3×100 mL) and a saturated NaCl solution (2×100 mL), dried (Na2SO4) and concentrated under reduced pressure. The residue was purified by column chromatography (10% EtOAc/90% hexane) to afford 4-(3-ethoxycarbonylphenoxy)-1-nitrobenzene as an oil (38 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841330B2
Source datasetuspto-grants-2014_09
ORD IDord-c39189c055ba442e8e8daaf5071fa3a7
Source noteuspto-grants-2014_09