HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formamide → 5-Methoxy-1H-isoindole-1,3(2H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formamide | HCID 713 | — |
| Reactant | 5-Methoxy-1,3-dihydro-2-benzofuran-1,3-dione | HCID 639748 | — |
| Product | 5-Methoxy-1H-isoindole-1,3(2H)-dione | HCID 13152719 | 77% |
Reaction Steps
A mixture of 4-methoxyphthalic anhydride (27.8 g, 0.16 mol) and formamide (175 ml) was stirred and held at 210° C. for 5 hours and was then allowed to cool to room temperature overnight. The solid material was filtered off, washed sequentially with water (100 ml), 50% aqueous acetone (50 ml) and diethyl ether (200 ml) and sucked dry under reduced pressure to afford 4-methoxyphthalimide (21.3 g, 77%) as a pale yellow solid. 1H NMR (DMSO-d6) 11.15 (1H, br s), 7.74 (1H, d), 7.33-7.28 (2H, m), 3.92 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08530469B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-27f071f83ac0413aba0618360d7523cd |
| Source note | uspto-grants-2013_09 |