تفاعل #4442

ord-ed73af56968b4454b488f0c1be5537e4

معادلة التفاعل

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
المردود 85.9%
O=[N+]([O-])c1ccc(Cc2nc(-c3ccncc3)cs2)cc1
2-(p-Nitrobenzyl)-4-(4-pyridyl)thiazole
المردود 85.9%

المذيبات

ظروف التفاعل

درجة الحرارة
10°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىdid not exceed 40° C
  2. 2
    أخرىthe layers separated
  3. 3
    غسيلthe combined organic extracts were washed with brine (20 mL)
  4. 4
    تجفيفdried over magnesium sulfate
  5. 5
    تركيزconcentrated

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04725606uspto-grants-1988_02