HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 970652Generated: October 29, 2026
Methyl iodide → 7-amino-4-methyl-2H-1,4-benzoxazine
https://huagongshe.com/reaction/970652
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 7-Nitro-3,4-dihydro-2H-1,4-benzoxazine | HCID 18416151 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-amino-4-methyl-2H-1,4-benzoxazine | HCID 11217429 | 95.4% |
Reaction Steps
Potassium carbonate (800 mg, 6 mmol) and methyl iodide (1.3 g, 9 mmol) were added to a solution of 3,4-dihydro-7-nitro-2H-benzo[b][1,4]oxazine (540 mg, 3 mmol) in DMF (10 mL). The reaction mixture was stirred at room temperature overnight. Sodium hydride (100 mg, 95%) and methyl iodide (1.0 g) were added and the reaction mixture was stirred at room temperature overnight. The solvent was removed under vacuum and the residue was suspended in water. A solid precipitated which was filtered and washed with water. The bright yellow solid was then suspended in MeOH (20 mL) and Pd/C (10%) was added. The suspension was stirred under an atmosphere of hydrogen overnight, then filtered through celite and the filtrate concentrated under vacuum to give the product (470 mg) as a purple oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07312233B2 |
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| Source dataset | uspto-grants-2007_12 |
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| ORD ID | ord-f1839c26ae8f4e118a78db9a98a785ef |
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| Source note | uspto-grants-2007_12 |
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