Hydrogen Peroxide → HCID 18432920, Verbindung

HRID 2305433

Reaktionsgleichung

Reaktionsgleichung von HRID 2305433
[NH2:1][C:2]1[C:7]([Br:8])=[C:6]([CH3:9])[C:5]([Br:10])=[CH:4][N:3]=1.OO.[OH2:13].[OH-:14].[Na+]>S(=O)(=O)(O)O>[N+:1]([C:2]1[C:7]([Br:8])=[C:6]([CH3:9])[C:5]([Br:10])=[CH:4][N:3]=1)([O-:14])=[O:13]

Komponenten

6

Reaktionsbedingungen

Temperatur
10 °C

Versuchsvorschrift

2-amino-3,5-dibromo-4-methylpyridine (8 g, 30.0 mmol) was cooled to 10° C., followed by the addition of concentrated sulfuric acid(10 ml). The mixture was stirred, maintaining the temperature at 10° C. for 2 hrs, with the addition of a mixture of 30% hydrogen peroxide in 30% fuming sulfuric acid(25 ml/50 ml). The mixture was allowed to warm to room temperature and stirred for an additional 48 hrs. The reaction was then added to 300 ml of water with cooling and made very slightly basic with dropwise addition of 505 NaOH solution while the temperature was maintained at 20-25° C. The product was extracted using ether(4×150 ml) and dried with MgSO4. The solution was concentrated and purified by flash chromatography(2% MeOH/CH2Cl2) to give the desired product(2.94 g, 33%). 1H NMR (CDCl3): δ 8.45 (s, 1H), 2.68 (s, 3H).

Aufarbeitung

  1. temperatureto warm to room temperature
  2. stirringstirred for an additional 48 hrs
  3. temperaturewith cooling
  4. temperaturewas maintained at 20-25° C
  5. extractionThe product was extracted
  6. dry with materialdried with MgSO4
  7. concentrationThe solution was concentrated
  8. custompurified by flash chromatography(2% MeOH/CH2Cl2)

Quellen und Nachweise

ORD-Eintrag
ord-fd6d09fb33ff48128f9350f020870d4b
Quelldatensatz
uspto-grants-2002_08
Patentnummer
US06440993B1

Verknüpfte Notizen

Wird geladen…