HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Carboxy-5-nitrobenzeneacetamide → 6-nitroisoquinoline-1,3(2H,4H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Carboxy-5-nitrobenzeneacetamide | HCID 59300036 | — |
| Solvent | 1,2-Dichlorobenzene | HCID 7239 | — |
| Product | 6-nitroisoquinoline-1,3(2H,4H)-dione | HCID 59299967 | 72.2% |
Reaction Steps
A stirred suspension of 11.1 g (49.3 mmol) of 2-carboxy-5-nitrobenzeneacetamide in 99 ml of 1,2-dichlorobenzene is refluxed for 3 h. The residue obtained after evaporation of the solvent under vacuum is washed with ether and dried to give 7.34 g (72%) of a tan solid, mp 255-260° (dec); 1H NMR (DMSO-d6) δ 11.6 (s, 1H), 8.2-8.3 (m, 3H), 4.17 (s, 2H); MS (ES−) m/z 205.2 (M−H)−
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07713994B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-883b462a15c642618599de7d8422cbdc |
| Source note | uspto-grants-2010_05 |