Reaktion #2396977

ord-c6229dce7f8546ebbbe7b90688fffed5

Reaktionsgleichung

O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
O=[N+]([O-])O
nitric acid
c1ccc(Cc2nc(-c3ccncc3)cs2)cc1
2-benzyl-4-(4-pyridyl)thiazole
O=S(=O)(O)O
sulfuric acid
O=[N+]([O-])c1ccc(Cc2nc(-c3ccncc3)cs2)cc1
crude product
Ausbeute 85.9%
O=[N+]([O-])c1ccc(Cc2nc(-c3ccncc3)cs2)cc1
2-(p-Nitrobenzyl)-4-(4-pyridyl)thiazole
Ausbeute 85.9%

Lösungsmittel

Reaktionsbedingungen

Temperatur
10°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigedid not exceed 40° C
  2. 2
    Sonstigethe layers separated
  3. 3
    Waschenthe combined organic extracts were washed with brine (20 mL)
  4. 4
    Trocknendried over magnesium sulfate
  5. 5
    Einengenconcentrated

Vorschrift

A solution of 2-benzyl-4-(4-pyridyl)thiazole (4.50 g, 0.018 mol) in chloroform (25 mL) was added dropwise to concentrated sulfuric acid (15 mL). The resulting mixture was cooled to 10° C. and fuming nitric acid (1.45 g, 0.97 mL) carefully added dropwise such that the reaction temperature did not exceed 40° C. The mixture was allowed to stir for thirty minutes, carefully neutralized with saturated sodium carbonate and the layers separated. The aqueous layer was reextracted with chloroform (2×25 mL) and the combined organic extracts were washed with brine (20 mL), dried over magnesium sulfate, and concentrated to afford a crude product (4.6 g). Several recrystallizations from hexane/ethyl acetate afforded pure 2-(p-nitrobenzyl)-4-(4-pyridyl)thiazole. mp. 140°-142° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04697012uspto-grants-1987_09