Sulfuric Acid → 3-Benzyloxy-5-hydroxypyridine

HRID 2305714Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2305714
[C:1]1([CH2:7][O:8][C:9]2[CH:10]=[C:11](N)[CH:12]=[N:13][CH:14]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.S(=O)(=O)(O)[OH:17].N([O-])=O.[Na+].[OH-].[Na+].[Na+].[Cl-]>O>[C:1]1([CH2:7][O:8][C:9]2[CH:10]=[C:11]([OH:17])[CH:12]=[N:13][CH:14]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Komponenten

7

Versuchsvorschrift

The 5-(phenylmethoxy)-3-pyridylamine (1.61 g, 8.00 mmol) was stirred into concentrated sulfuric acid (1.7 mL), water (2.5 mL) and ice (4 g). This mixture was allowed to stir for 10 min until the solution became homogeneous. To this cold, stirring solution was added a solution of sodium nitrite (552 mg, 8.00 mmol) in water (2 mL). The mixture was allowed to stir for 10 min. A boiling solution of concentrated sulfuric acid (5 mL) and water (4 mL) was added. The mixture was heated until all solids dissolved. Ice was added to cool the reaction. The pH was adjusted to 8 with 10% NaOH solution and saturated NaCl solution was added. The product was extracted with ethyl acetate (4×100 mL). The combined ethyl acetate extracts were dried (Na2SO4), filtered, concentrated by rotary evaporation and briefly vacuum to give 1.52 g (94.4%).

Aufarbeitung

  1. stirringTo this cold, stirring solution
  2. stirringto stir for 10 min
  3. temperatureThe mixture was heated until all solids
  4. dissolutiondissolved
  5. additionIce was added
  6. temperatureto cool
  7. customthe reaction
  8. additionwas added
  9. extractionThe product was extracted with ethyl acetate (4×100 mL)
  10. dry with materialThe combined ethyl acetate extracts were dried (Na2SO4)
  11. filtrationfiltered
  12. concentrationconcentrated by rotary evaporation and briefly vacuum
  13. customto give 1.52 g (94.4%)

Quellen und Nachweise

ORD-Eintrag
ord-cc8d744e91514fb79c5e9d8619725ce3
Quelldatensatz
uspto-grants-2002_08
Patentnummer
US06441006B2

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