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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376024Generated: October 31, 2026

Ethanol → 3-Ethoxy-2,4,5-trifluorobenzoic acid

https://huagongshe.com/reaction/376024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTetrafluorophthalic anhydrideHCID 69545—
ReactantLithium hydroxide, monohydrateHCID 168937—
SolventWaterHCID 962—
Product3-Ethoxy-2,4,5-trifluorobenzoic acidHCID 1063269477.5%

Reaction Conditions

Temperature140 °C

Reaction Steps

4.4 g (20 mmol) of tetrafluorophthalic anhydride are dissolved in 3 g of water and 30 g of ethanol, 4.2 g of lithium hydroxide hydrate are added, and the mixture is heated at reflux for 48 hours. Then 50 g of water are added and an ethanol/water mixture (31.9 g) is distilled off until a head temperature of 100° C. is reached. Subsequently a pH of 0.6 is established by adding 19 g of 30% strength hydrochloric acid, and the mixture is extracted using a mixture of 20 g of 1,2-dichlorobenzene and 10 g of Hostarex A327. The organic phase is dried over MgSO4, heated at 140° C. for one hour until the evolution of gas comes to an end (decarboxylation) and then adjusted at 25° C. to a pH of 14 using 12.1 g of 35% strength sodium hydroxide solution. The mixture is extracted three times with in each case 50 g of dichloromethane, and the aqueous phase is adjusted to a pH of 0.7 by adding 9.4 g of 30% strength hydrochloric acid and extracted with MTBE. The mixture is dried over MgSO4 and filtered, and removal of the solvent leaves 3.4 g (15.5 mmol, corresponding to 77%) of yellowish 3-ethoxy-2,4,5-trifluorobenzoic acid (purity by GC>95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05488152
Source datasetuspto-grants-1996_01
ORD IDord-8a9413beaee14fc08321506db700bcde
Source noteuspto-grants-1996_01