HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formamide → 4-Methoxyisoindoline-1,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formamide | HCID 713 | — |
| Reactant | 4-Methoxy-1,3-dihydro-2-benzofuran-1,3-dione | HCID 291193 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Methoxyisoindoline-1,3-dione | HCID 16638228 | 37% |
Reaction Steps
A mixture of 3-methoxyphthalic anhydride (24.0 g, 134.8 mmol) and formamide (120 ml) was stirred and held at 210° C. for 5 hours and was then allowed to cool to room temperature overnight. Water (100 ml) was added and the solid material filtered off under reduced pressure. The crude product was washed sequentially with 50% aqueous acetone (50 ml) and diethyl ether (200 ml) and sucked dry under reduced pressure to afford 3-methoxyphthalimide (8.95 g, 37%) as an off-white solid. 1H NMR (DMSO-d6) 11.08 (1H, br s), 7.78 (1H, dd), 7.45 (1H, d), 7.36 (1H, d), 3.93 (3H, s). MS: [M+H]+ 178.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08101648B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-72be81a7801c49fd89559a9f8c568ae4 |
| Source note | uspto-grants-2012_01 |