Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus trichloride | HCID 24387 | — |
| Reactant | 2,3-Dimethyl-4-nitropyridine-N-oxide | HCID 148223 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,3-Dimethyl-4-nitropyridine | HCID 11217348 | 95% |
Reaction Steps
2,3-Dimethyl-4-nitropyridin-N-oxide (75.6 g, 0.45 mol) prepared in Step 1 was dissolved in 300 ml of methylene chloride. A solution of phosphorus trichloride (44 ml) in methylene chloride (60 ml) was slowly added to the solution for 30 minutes at −15° C.˜−20° C. The reaction mixture was stirred for 15 minutes at the same temperature and further stirred for 15 minutes at room temperature. The reaction mixture was cooled to −78° C. 50 ml of water was added to the reaction mixture, which was neutralized with a sodium hydroxide solution and then extracted with methylene chloride. The separated organic layer was dried on anhydrous magnesium sulfate and then concentrated under reduced pressure to give the titled compound as a pale yellow solid (65 g, 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07642269B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-a2920229c62f4df39ff28c32324b4d0d |
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| Source note | uspto-grants-2010_01 |
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