HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553545Generated: October 26, 2026
Dimethylformamide → HCID 59340050, compound
https://huagongshe.com/reaction/553545
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Bromoisatoic anhydride | HCID 11521577 | — |
| Reactant | HCID 59340108 | HCID 59340108 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 59340050 | HCID 59340050 | 74% |
Reaction Steps
7-Bromo-1-methyl-1H-benzo[d][1,3]oxazine-2,4-dione. Sodium hydride (0.47 g, 12 mmol) was added to a 3 neck 250 mL round bottom flask under nitrogen and then washed with hexanes. Once the hexanes were decanted, DMF (20.0 mL, 11 mmol) was added. The resulting mixture was cooled to 0° C. using an ice-water bath, and then 7-bromo-1H-benzo[d][1,3]oxazine-2,4-dione (2.7 g, 11 mmol) was added in one batch. After stirring at room temperature for 1 hour, iodomethane (0.70 mL, 11 mmol) was added dropwise to the yellow solution, and the reaction mixture was stirred for 16 hours. Water (50 mL) was added, and the resulting precipitate that formed was collected via filtration. The solid was washed with additional water (100 mL), followed by ether (100 mL). Drying in a vacuum oven overnight at 50° C. provided the title compound as an off-white solid (2.1 g, 74% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08048894B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-c49bd567fb9747fcab1326c636d8d23c |
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| Source note | uspto-grants-2011_11 |
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