Stannous chloride dihydrate → 2-Chloro-5-(trifluoromethyl)pyridin-3-amine

HRID 1929452Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1929452
[Cl:1][C:2]1[C:7]([N+:8]([O-])=O)=[CH:6][C:5]([C:11]([F:14])([F:13])[F:12])=[CH:4][N:3]=1.O.O.[Sn](Cl)Cl.C(=O)([O-])O.[Na+]>C(OCC)(=O)C>[NH2:8][C:7]1[C:2]([Cl:1])=[N:3][CH:4]=[C:5]([C:11]([F:13])([F:12])[F:14])[CH:6]=1

Komponenten

5

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

To a solution of 2-chloro-3-nitro-5-(trifluoromethyl)pyridine (1.87 g) in ethyl acetate (40 mL) was added tin(II) chloride dihydrate (8.22 g), and the mixture was stirred at 80° C. for 2 hours. After cooling, to the reaction mixture was added an aqueous saturated sodium hydrogencarbonate solution, and the mixture was vigorously stirred at room temperature and filtered through a celite pad. The residue was washed with ethyl acetate. The filtrate was combined with the washings, washed successively with an aqueous saturated sodium hydrogencarbonate solution, water and brine, dried over sodium sulfate and concentrated in vacuo. The resultant residue was triturated with n-hexane to give 3-amino-2-chloro-5-(trifluoromethyl)pyridine (0.99 g) as a pale yellow powder.

Aufarbeitung

  1. temperatureAfter cooling, to the reaction mixture
  2. stirringthe mixture was vigorously stirred at room temperature
  3. filtrationfiltered through a celite pad
  4. washThe residue was washed with ethyl acetate
  5. washwashed successively with an aqueous saturated sodium hydrogencarbonate solution, water and brine
  6. dry with materialdried over sodium sulfate
  7. concentrationconcentrated in vacuo
  8. customThe resultant residue was triturated with n-hexane

Quellen und Nachweise

ORD-Eintrag
ord-0bca277732da453aad68302d58121113
Quelldatensatz
uspto-grants-2012_05
Patentnummer
US08188073B2

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