Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Oxazine | HCID 12313776 | — |
| Product | Nitro-oxazine | HCID 66992931 | — |
Reaction Steps
The oxazine of formula XI (0.1 mmol) was added portionwise to concentrated sulfuric acid (2 ml) at 22° C. The solution obtained was cooled to 0° C. and treated with red fuming nitric acid (0.058 ml) and stirring was continued at 0° C. for 2 hours. For the workup, the reaction mixture was slowly added to crushed ice and the pH was adjusted to 10 using a saturated solution of sodium carbonate. The aqueous layer was extracted with ethyl acetate, the organic layer was dried over sodium sulphate and evaporated to afford the pure nitro-oxazine of formula XII. Alternatively, the crude product was purified by flash chromatography on silica-NH2 gel using mixtures of heptane or cyclohexane and ethyl acetate as the eluent to yield the pure nitro-oxazines of formula XII.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181232B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-a21b592817f545dc934d640782bcbe98 |
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| Source note | uspto-grants-2015_11 |
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