HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2-(2,4,6-Trifluorophenyl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 3,4,5,6-Tetrahydrophthalic anhydride | HCID 12475 | — |
| Reactant | 2,4,6-Trifluoroaniline | HCID 67765 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(2,4,6-Trifluorophenyl)-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione | HCID 21426811 | — |
Reaction Steps
A solution of 5.3 parts of 3,4,5,6-tetrahydrophthalic anhydride in 100 parts of glacial acetic acid was treated with 5 parts of 2,4,6-trifluoroaniline at once. After refluxing for 24 hours, the acetic acid was stripped from the reaction mixture under 300 mm Hg. pressure. The residue was dissolved in 100 parts of methylene chloride and washed with 100 parts of 10% aqueous sodium carbonate solution. After drying over anhydrous sodium sulfate, the solution was stripped under 300 mm Hg. pressure. The resulting pink oil was crystallized from 70 parts of methanol at -40° C. to yield 4.7 parts white crystals of 2-(2,4,6-trifluorophenyl)-4,5,6,7-tetrahydro-2H-isoindole-1,3-dione melting at 91°-92° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04032326 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-c7a1a38b99904617a1fdf4517e9e8363 |
| Source note | uspto-grants-1977_06 |