Tetrahydrofuran → 3-Chloro-6-methoxypyridazine

HRID 454821

Reaktionsgleichung

Reaktionsgleichung von HRID 454821
CO.C[O-].[Na+].[O:6]1CCC[CH2:7]1.[Cl:11][C:12]1[N:13]=[N:14][C:15](Cl)=[CH:16][CH:17]=1>O>[CH3:7][O:6][C:15]1[N:14]=[N:13][C:12]([Cl:11])=[CH:17][CH:16]=1

Komponenten

5

Edukt 3

HCID 8028TetrahydrofuranHCID 673313,6-DichloropyridazineHCID 23694274Sodium methanolate methanol

Produkt 1

HCID 744033-Chloro-6-methoxypyridazineAusbeute 90 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

A 0.5 M sodium methoxide methanol solution (NaOMe in MeOH, 7.4 mL, 3.69 mmol) was slowly added to an anhydrous tetrahydrofuran (12 mL) solution having 3,6-dichloropyridazine (107, 500 mg, 3.36 mmol) dissolved therein, stirred at room temperature for one hour, followed by adding water. Organic compounds were extracted with ethyl acetate. Then, the recovered organic solution was washed with an aqueous solution of saturated sodium chloride and evaporated after a treatment with sodium sulfate. Purification was performed by column chromatograph to give the target compound 3-methoxy-6-chloropyridazine (108a, 436 mg, 90%) as a white solid.

Aufarbeitung

  1. dissolutiondissolved
  2. extractionOrganic compounds were extracted with ethyl acetate
  3. washThen, the recovered organic solution was washed with an aqueous solution of saturated sodium chloride
  4. customevaporated after a treatment with sodium sulfate
  5. customPurification

Quellen und Nachweise

ORD-Eintrag
ord-f94eb002897047a8bebf9c0993e81a45
Quelldatensatz
uspto-grants-2013_07
Patentnummer
US08497260B2

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