HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326585Generated: October 30, 2026
Bicarbonate Ion → HCID 10755399, compound
https://huagongshe.com/reaction/326585
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bicarbonate Ion | HCID 769 | — |
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 10752413 | HCID 10752413 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 10755399 | HCID 10755399 | — |
Reaction Steps
2,2-Dimethyl-4-(2-pyridyl)-2H-1,3-benzoxazine (0.50 g) was dissolved in acetic acid (1 ml) and to the solution was added conc. sulfuric acid (3 ml) with ice-cooling. Conc. nitric acid (0.2 ml) was then added to the mixture, and the mixture was stirred for 10 minutes with ice-cooling. The reaction mixture was added slowly to a thoroughly cooled mixture of an aqueous 5N sodium hydroxide solution (50 ml) and saturated bicarbonate solution (20 ml) to quench the reaction. The mixture was extracted by addition of ethyl acetate. The mixture was successively washed with an aqueous sodium bicarbonate solution and saturated saline solution and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the residue was crystallized from hexane to obtain 6-nitro-2,2-dimethyl-4-(2-pyridyl)-2H-1,3-benzoxazine (0.58 g) (Compound 11).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05270308 |
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| Source dataset | uspto-grants-1993_12 |
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| ORD ID | ord-b62e1749aecf441ab6c150863a28237d |
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| Source note | uspto-grants-1993_12 |
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