HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 178472903, compound → ethyl 6-iodo-4-oxo4H-1,2-benzoxazine-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 178472903 | HCID 178472903 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | ethyl 6-iodo-4-oxo4H-1,2-benzoxazine-3-carboxylate | HCID 22397138 | 52.9% |
Reaction Steps
A solution of ethyl 3-(2-fluoro-5-iodophenyl)-2-(hydroxyimino)-3-oxopropanoate (Preparation 16, 1.3 g) in toluene (20 mL) is heated to reflux under nitrogen for 48 h. The reaction mixture is cooled to room temperature and concentrated in vacuo to give 1.33 g of a crude yellow solid which is recrystallized from ether to afford 0.65 g of the title compound as a yellow crystalline solid. Physical characteristics: mp 130-131: 1H NMR (300 MHz, CDCl3) δ 1.45, 4.51, 7.35, 8.09, 8.50; IR (drift) 2475, 2425, 2382, 2350, 2260, 1742, 1663, 1456, 1332, 1240, 1195, 1150, 1010, 987, 831 cm−1; HRMS (FAB) m/z 345.9581 (C11H8INO4+H). Anal. Found: C, 38.03; H, 2.52; N, 4.06.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06559145B2 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-643ca014295544f68ee9549871045048 |
| Source note | uspto-grants-2003_05 |