HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981295Generated: October 30, 2026
Methyl iodide → 5-methoxy-1-methyl-2H-3,1-benzoxazine-2,4(1H)-dione
https://huagongshe.com/reaction/981295
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Methoxy-2H-3,1-benzoxazine-2,4(1H)-dione | HCID 10750295 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-methoxy-1-methyl-2H-3,1-benzoxazine-2,4(1H)-dione | HCID 15480194 | 80.7% |
Reaction Steps
To a stirred and cooled (<10° C.) solution of 9.65 parts of 5-methoxy-2H-3,1-benzoxazine-2,4(1H)-dione in 54 parts of N,N-dimethylformamide were added portionwise 2.64 parts of a sodium hydride dispersion 50%. After stirring for 1 hour in an ice bath. 7.81 parts of iodomethane were added dropwise at <15° C. When the reaction mixture was solidified, 45 parts of N,N-dimethylformamide were added and a sodium hydride dispersion 50% was further added dropwise. Upon complete addition, stirring was continued overnight while the reaction mixture was allowed to reach room temperature. The reaction mixture was poured into ice water and 2,2'-oxybispropane was added. The precipitated product was filtered off, washed with water and dried, yielding 8.37 parts (80.7%) of 5-methoxy-1-methyl-2H-3,1-benzoxazine-2,4(1H)-dione; mp. 215.8° C. (interm. 2)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04990521 |
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| Source dataset | uspto-grants-1991_02 |
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| ORD ID | ord-d895623cfa69427487b16d3414c9b874 |
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| Source note | uspto-grants-1991_02 |
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