HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2,4-Trichlorobenzene → 1,3-Isobenzofurandione, 5-fluoro-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2,4-Trichlorobenzene | HCID 13 | — |
| Reactant | 5,5-Difluorohexahydro-2-benzofuran-1,3-dione | HCID 14008249 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | 1,3-Isobenzofurandione, 5-fluoro- | HCID 67572 | 51% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04517372 |
| Source dataset | uspto-grants-1985_05 |
| ORD ID | ord-7a715e5aea7c40bd84490c2c2b6c08ca |
| Source note | uspto-grants-1985_05 |