HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 2,2,4-trimethyl-6-nitro-2H-1,4-benzoxazin-3(4H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,2-Dimethyl-6-nitro-2H-benzo[B][1,4]oxazin-3(4H)-one | HCID 10656631 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2,2,4-trimethyl-6-nitro-2H-1,4-benzoxazin-3(4H)-one | HCID 13665543 | — |
Reaction Steps
2,2-Dimethyl-6-nitro-4H-benzo[1,4]oxazin-3-one (1.1 g) was mixed with MeI (850 mg, Aldrich), K2CO3 (1.38 g, Aldrich) and DMF (30 ml, Aldrich) at 40° C. for 48 h. The DMF was removed in vacuo and the residue was diluted with EtOAc (80 ml). The organic phase was washed with H2O (50 ml), aqueous Na2SO3 (50 ml) and brine (50 ml). The resulting solution was dried (MgSO4) and concentrated to provide the compound which was used as is.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08642624B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-084d1642d0904ad5a1a2113cf8258135 |
| Source note | uspto-grants-2014_02 |