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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462822Generated: October 29, 2026

1,2,4-Trichlorobenzene → 1,3-Isobenzofurandione, 5-fluoro-

https://huagongshe.com/reaction/462822

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2,4-TrichlorobenzeneHCID 13—
Reactant5,5-Difluorohexahydro-2-benzofuran-1,3-dioneHCID 14008249—
CatalystPalladiumHCID 23938—
Product1,3-Isobenzofurandione, 5-fluoro-HCID 6757251%

Reaction Steps

A mixture of 500 parts of 4,4-difluorohexahydrophthalic anhydride and 100 parts of 5 percent Pd/C catalyst in 3615 parts of 1,2,4-trichlorobenzene was charged to an autoclave reactor. The autoclave atmosphere was purged with nitrogen. The autoclave was then sealed, heated to about 250°-285° C. and maintained thereat for about 3.5 hours, then cooled to about room temperature. Analysis of the reaction product by gas chromatographic techniques, indicated a yield of about 51 percent 4-fluorophthalic anhydride, based on the difluorohexahydrophthalic anhydride reactant.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04517372
Source datasetuspto-grants-1985_05
ORD IDord-7a715e5aea7c40bd84490c2c2b6c08ca
Source noteuspto-grants-1985_05