Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Phenyl 2-bromo-2-propyl ketone | HCID 66324 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 2-Amino-5-Nitrophenol | HCID 4984721 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 66790190 | HCID 66790190 | 66.4% |
Reaction Steps
To a suspension of 2-amino-5-nitrophenol (3.00 g) in N,N-dimethyl-formamide (30 mL) was added potassium fluoride (3.40 g), and the mixture was stirred at room temperature for 15 minutes, and thereto was added 2-bromo-2-methylpropiophenone (4.42 g). The mixture was stirred at room temperature for 0.5 hour, at 60° C. for 20 hours and at 80° C. for 3 days. After cooling, to the reaction mixture was added cold water, and the mixture was extracted with ethyl acetate. The organic layer was washed successively with water and brine, dried over sodium sulfate and concentrated in vacuo. The resultant residue was purified by column chromatography on silica gel (solvent; n-hexane/ethyl acetate=10/1) to give 2,2-dimethyl-7-nitro-3-phenyl-2H-1,4-benzoxazine (3.65 g) as a pale yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188073B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-b18aea0730994a8182b476917d5d6ddb |
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| Source note | uspto-grants-2012_05 |
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