HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 6-Fluoro-1-methyl-2H-3,1-benzoxazine-2,4(1H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Fluoroisatoic anhydride | HCID 288560 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Fluoro-1-methyl-2H-3,1-benzoxazine-2,4(1H)-dione | HCID 12713230 | 57% |
Reaction Steps
A solution of Compound 35 (3 g, 16.57 mmol) in DMF was added slowly to a suspension of NaH (60% in mineral oil, 0.729 g, 18.23 mmol) in DMF and further stirred at room temperature for 1 h. Then, neat methyl iodide (1.14 mL, 18.23 mmol) was added and the solution further stirred at room temperature for 3 h. The solution was poured into ice water and the solids formed were filtered, washed several times by water, and dried. The solids were suspended in hexane, sonicated briefly, filtered, and washed by hexane to yield 1.84 g (57%) of white solids. M.P. 133° C. 1H NMR (DMSO-d6): δ3.90 (s, 3H), 7.51 (dd, J=4.0, 8.8 Hz, 1H), 7.77 (m, 12). Anal. (C9H6FNO3) C, H, N.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07173036B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-74ef3fd4f2ea4b88a34126a27348bcb7 |
| Source note | uspto-grants-2007_02 |