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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339511Generated: October 30, 2026

Hydrochloric Acid → 4-(3,3,3-Trifluoropropoxy)benzoic acid

https://huagongshe.com/reaction/339511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHydrogen PeroxideHCID 784—
ReactantPotassium HydroxideHCID 14797—
Reactant4-(3,3,3-Trifluoropropoxy)benzaldehydeHCID 58342188—
SolventMethanolHCID 887—
Product4-(3,3,3-Trifluoropropoxy)benzoic acidHCID 5811165583%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a stirred solution of 50% w/v KOH (0.8 ml) and 4-(3,3,3-trifluoropropoxy)benzaldehyde (0.4 g, 1.83 mmol) in MeOH (4 ml) at 65° C. was added dropwise over 20 min aqueous hydrogen peroxide (30 wt. % in water, 1.5 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 (3×25 ml). The combined organic extracts were washed with brine (25 ml), dried (Na2SO4) and the solvent removed under reduced pressure to give the title compound (0.36 g, 83%) as a colourless solid which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895313B2
Source datasetuspto-grants-2014_11
ORD IDord-3ddbd9232e7c4b4c9a40e16e6fa7bf6c
Source noteuspto-grants-2014_11