HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dibromoethane → 7-Methyl-3,4-dihydro-2H-1,4-benzoxazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Amino-5-methylphenol | HCID 76082 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-Methyl-3,4-dihydro-2H-1,4-benzoxazine | HCID 12510545 | — |
Reaction Conditions
| Temperature | 130 °C |
|---|
Reaction Steps
To a solution of 2-amino-5-methylphenol (5.0 g) in N,N-dimethylformamide (50 ml), potassium carbonate (28.3 g) and 1,2-dibromoethane (10.6 ml) were added and stirred at 130° C. for 11 hours. After insoluble materials were filtered off, the filtrate was diluted with ethyl acetate and washed sequentially with water and brine. The organic layer was dried over anhydrous sodium sulfate and then filtered to remove the desiccant, followed by distilling off the solvent under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluting solvent: n-hexane:ethyl acetate=20:1 to 9:1) to give the titled compound, i.e., 7-methyl-3,4-dihydro-2H-1,4-benzoxazine (980 mg) as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08222417B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-56e45d5e28934131adb0e0f50448e64c |
| Source note | uspto-grants-2012_07 |