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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591113Generated: October 23, 2026

Water → 2,4,5-Trifluorophenylacetic acid

https://huagongshe.com/en/reaction/591113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSulfuric AcidHCID 1118—
Reactanttert-Butyl methyl etherHCID 15413—
ReactantHCID 86343656HCID 86343656—
Product2,4,5-Trifluorophenylacetic acidHCID 277795025%

Reaction Conditions

Temperature100 °C

Reaction Steps

50 ml of concentrated sulphuric acid was added to 1-chloroethynyl-2,4,5-trifluorobenzene of formula IV, X=Cl and the mixture heated to 100° C. and left to stir for 1 hour. 50 ml of MTBE and 100 ml of water were then added. The phases were separated and the aqueous phase was re-extracted with 2×50 ml of MTBE. The combined organic phases were counter extracted with 3×50 ml of aqueous NaHCO3 and put to one side. The three aqueous phases of NaHCO3 were recombined and the resulting phase was acidified with hydrochloric acid and then extracted with 3×50 ml of MTBE. The organic phases were concentrated to a residue obtaining 0.25 g of 2,4,5-trifluorophenylacetic acid of formula (I) with a molar yield of 25%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238613B2
Source datasetuspto-grants-2016_01
ORD IDord-595be5e545694559902aec5983a04aa2
Source noteuspto-grants-2016_01