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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1589942Generated: November 1, 2026

Ethyl Acetate → 3,4,6-Trifluorophthalic anhydride

https://huagongshe.com/reaction/1589942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
ReactantTetrafluorophthalic anhydrideHCID 69545—
ReactantHCID 10130673HCID 10130673—
CatalystZincHCID 23994—
SolventWaterHCID 962—
SolventO-XyleneHCID 7237—
Product3,4,6-Trifluorophthalic anhydrideHCID 9815604—

Reaction Conditions

Temperature100 °C

Reaction Steps

5.5 g (25 mmol) of tetrafluorophthalic anhydride were added under nitrogen to a solution of 3.58 g (89.5 mmol) of sodium hydroxide in 30 g of water. The mixture was then heated at 100° C., and 6.54 g (0.1 mol) of zinc dust were added. The course of the reaction was monitored by GC(TLC), and the reaction was complete after 12 hours. 50 ml portions of water and ethyl acetate were added and the voluminous solids were filtered off with suction and washed four times with 50 ml portions of water. The colorless filtrate was brought to a pH of 1 and extracted using ethyl acetate. Drying of the organic phases over MgSO4, filtration and removal of the solvent in vacuo gave 4.72 g (22.2 mmol; 89%) of colorless powder which could be identified as 3,4,6-trifluorophthalic acid (melting point 156°-160° C). Azeotropic dehydration in boiling xylene gave 3,4,6-trifluorophthalic anhydride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05200556
Source datasetuspto-grants-1993_04
ORD IDord-b280b8fd425b4a68947efb3632b3b3b6
Source noteuspto-grants-1993_04