HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 7-Fluoro-2-methylisatoicanhydride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 7-Fluoroisatoic anhydride | HCID 10058138 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 7-Fluoro-2-methylisatoicanhydride | HCID 10330274 | — |
Reaction Steps
A stirred solution of 7-fluoro-1H-3,1-benzoxazine-2,4-dione (9.0 g) in dimethylacetamide (100 ml) at 18.5° was treated portionwise with sodium hydride (80% dispersion in mineral oil, 1.65 ) during 10 minutes. The mixture was stirred for a further 75 minutes. Methyl iodide (7.81 g) was then added dropwise to the stirred mixture during 5 minutes and the mixture was stirred for a further 18.5 hours at ambient temperature. Solvent (60 ml) was removed by distillation in vacuo. The residue was cooled to 3° and poured into ice-water. The resulting precipitate was collected, dried in vacuo and recrystallised from dichloromethane to give 7-fluoro-1-methyl-1H-3,1-benzoxazine-2,4-dione m.p. 158°-159.5°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04659718 |
| Source dataset | uspto-grants-1987_04 |
| ORD ID | ord-ef26692064e547e8a0e4e3b85480da65 |
| Source note | uspto-grants-1987_04 |