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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339507Generated: October 27, 2026

Hydrochloric Acid → 2-methoxy-5-(trifluoromethoxy)benzoic Acid

https://huagongshe.com/reaction/339507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHydrogen PeroxideHCID 784—
ReactantPotassium HydroxideHCID 14797—
Reactant2-Methoxy-5-(trifluoromethoxy)benzaldehydeHCID 2783364—
SolventMethanolHCID 887—
Product2-methoxy-5-(trifluoromethoxy)benzoic AcidHCID 277528691%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a stirred solution of 2-methoxy-5-trifluoromethoxybenzaldehyde (2.0 g, 9.09 mmol) and 50% KOH (4.1 ml) in MeOH (15 ml) at 65° C. was added dropwise hydrogen peroxide (30%, 7.4 ml) over 20 min. The reaction mixture was then stirred at 65° C. for 10 min., cooled to room temperature, acidified with 1 M HCl, and extracted with Et2O (3×40 ml). The combined organic extracts were washed with brine (35 ml), dried (Na2SO4) and the solvent removed under reduced pressure to give a pale yellow viscous oil which solidified at room temperature overnight to give the title compound (1.95 g, 91%) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895313B2
Source datasetuspto-grants-2014_11
ORD IDord-42d02c996db540dcaa03b8c4c3c23326
Source noteuspto-grants-2014_11