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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553545Generated: October 26, 2026

Dimethylformamide → HCID 59340050, compound

https://huagongshe.com/reaction/553545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant4-Bromoisatoic anhydrideHCID 11521577—
ReactantHCID 59340108HCID 59340108—
SolventWaterHCID 962—
ProductHCID 59340050HCID 5934005074%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048894B2
Source datasetuspto-grants-2011_11
ORD IDord-c49bd567fb9747fcab1326c636d8d23c
Source noteuspto-grants-2011_11