Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 86223896 | HCID 86223896 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | HCID 86223897 | HCID 86223897 | — |
Reaction Steps
2,6-Bis-(2,2,2-trifluoro-ethyl)-pyridine 1-oxide (2.65 g, 10.22 mmol) was dissolved in H2SO4 (4 mL) and cooled to 0° C. HNO3 (3.2 mL) was added slowly and after the addition was complete the reaction mixture was heated to 90° C. for 2 hours. The mixture was poured into ice, made basic with 15% NaOH and extracted with CH2Cl2. The organic layers were washed with brine, dried over Na2SO4 and concentrated to a red oil (2.72 g, 81%). 1H NMR (400 MHz, CDCl3): δ 3.95 (t, J=10.1 Hz, 4H), 8.31 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07622605B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-2b6a613f70b54e0a99a0aa23a8095186 |
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| Source note | uspto-grants-2009_11 |
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