Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339515Generated: October 25, 2026

Hydrochloric Acid → 4-(2-Fluoroethoxy)benzoic acid

https://huagongshe.com/reaction/339515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHydrogen PeroxideHCID 784—
ReactantPotassium HydroxideHCID 14797—
Reactant4-(2-Fluoroethoxy)benzaldehydeHCID 15058649—
SolventMethanolHCID 887—
Product4-(2-Fluoroethoxy)benzoic acidHCID 5135709363%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a stirred solution of 50% w/v KOH (1.3 ml) and 4-(2-fluoroethoxy)benzaldehyde (0.5 g, 2.98 mmol) in MeOH (6 ml) at 65° C. was added dropwise over 20 min aqueous hydrogen peroxide (30 wt. % in water, 2.45 ml). On completion of the addition the reaction mixture was heated at 65° C. for a further 10 min. On cooling to room temperature, the reaction mixture was acidified with 1 M HCl and extracted with Et2O (3×30 ml). The combined organic extracts were washed with brine (30 ml), dried (Na2SO4) and the solvent removed under reduced pressure to give a solid which was purified by flash chromatography (1:1 Hexane/EtOAc) to give the title compound (0.278 g, 63%) as a colourless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895313B2
Source datasetuspto-grants-2014_11
ORD IDord-db5125dd0639494b9ee21fc6a3c480e7
Source noteuspto-grants-2014_11