تفاعل #1954

ord-9c15659462ee47fb96bbf189ac58fe27

معادلة التفاعل

Cc1cc(Cl)c(F)c[n+]1[O-]
4-Chloro-5-fluoro-2-picoline-N-oxide
O=C([O-])[O-].[K+].[K+]
potassium carbonate
Cc1cc(Cl)c(F)cn1
title compound
المردود 142.1%
Cc1cc(Cl)c(F)cn1
4-Chloro-5-fluoro-2-picoline
المردود 142.1%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىequiped with a mechanical stirrer, a condenser
  2. 2
    درجة الحرارةthe reaction mixture was carefully heated to 35°-40° C
  3. 3
    أخرىan exothermic reaction
  4. 4
    أخرىto rise to 120° C.
  5. 5
    أخرىThe flask was transferred to a cold water bath
  6. 6
    workup.ADDITIONThe reaction mixture was then poured over ice
  7. 7
    workup.DISTILLATIONdistilled
  8. 8
    workup.DISTILLATIONThe aqueous distillate collected at 92°-96° C.
  9. 9
    استخلاصwas extracted with three portions of methylene chloride
  10. 10
    استخلاصThe combined organic extract
  11. 11
    تجفيفwas dried over anhydrous sodium sulfate
  12. 12
    ترشيحfiltered
  13. 13
    workup.DISTILLATIONdistilled

الإجراء التجريبي

4-Chloro-5-fluoro-2-picoline-N-oxide (12.43 g, 76.93 mmol), from Step 7, was dissolved in 52 mL of glacial acetic acid in a 3-necked flask equiped with a mechanical stirrer, a condenser and a thermometer. Iron powder (6.45 g, 115.5 mmol) was added to the solution at ambient temperature and the reaction mixture was carefully heated to 35°-40° C. After 10 min at 30° C., an exothermic reaction took place which caused the reaction temperature to rise to 120° C. and the reaction mixture became a very dark brown-colored solution. The flask was transferred to a cold water bath and the temperature of the solution brought down to ambient. The reaction mixture was then poured over ice. The resultant aqueous mixture was adjusted to pH 9 with potassium carbonate and steam distilled. The aqueous distillate collected at 92°-96° C. was extracted with three portions of methylene chloride. The combined organic extract was dried over anhydrous sodium sulfate, filtered and distilled to afford 15.91 g (71% yield) of the title compound, b.p. 138°-140° C.; MS GC-MS M/Z: 146 (M+H)+ ; 1H NMR (CDCl3) d 2.53 (s, 3H), 7.23 (d, 1H, J=6.0 Hz), 8.37 (s, 1H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05726182uspto-grants-1998_03