Potassium Carbonate → 6-Chloro-2,3-dimethylpyridine

HRID 603505Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 603505
[CH3:1][C:2]1[CH:3]=[CH:4][C:5](=O)[NH:6][C:7]=1[CH3:8].P(Cl)(Cl)([Cl:12])=O.P(Cl)(Cl)(Cl)(Cl)Cl.[OH-].[K+].C(=O)([O-])[O-].[K+].[K+]>C(Cl)Cl.O>[Cl:12][C:5]1[N:6]=[C:7]([CH3:8])[C:2]([CH3:1])=[CH:3][CH:4]=1

Komponenten

8

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

5,6-dimethyl-2(1H)pyridinone (Example 476, 0.39 g, 3.2 mmol) was suspended in phosphorous oxychloride (5.00 mL, 53.6 mmol) and heated to 100° C. Then, phosphorous pentachloride (4.00 g, 19.2 mmol) was added, and the mixture was heated to 140° C. After 16 h, the mixture was cooled to rt, diluted with CH2Cl2 (5 mL), and slowly poured into a 0° C. solution of potassium hydroxide (5 g) and potassium carbonate (5 g) in water (100 mL). Upon complete addition, the mixture was allowed to warm to rt and stirred for 1 h. The aqueous solution was extracted with CH2Cl2, and the combined organics layers were dried (MgSO4), filtered, and concentrated in vacuo to provide the title compound (0.35 g, 77%) as a brown oil. The material was used in the next step without further purification. 1H NMR (400 MHz, CDCl3) δ 7.36 (d, 1H), 7.07 (d, 1H), 2.49 (s, 3H), 2.27 (s, 3H).

Aufarbeitung

  1. temperaturethe mixture was heated to 140° C
  2. temperaturethe mixture was cooled to rt
  3. additionUpon complete addition
  4. temperatureto warm to rt
  5. extractionThe aqueous solution was extracted with CH2Cl2
  6. dry with materialthe combined organics layers were dried (MgSO4)
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-a271b07b76ef465b8659877fe5020b72
Quelldatensatz
uspto-grants-2011_03
Patentnummer
US07906653B2

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