تفاعل #1770834

ord-910721eee2544463b8c9a87942ea3b72

معادلة التفاعل

Cc1c(OCC(F)(F)C(F)(F)F)cc[n+]([O-])c1C
2,3-dimethyl-4-(2,2,3,3,3-pentafluoropropoxy)-pyridine-1-oxide
CC(=O)OC(C)=O
acetic anhydride
Cc1c(OCC(F)(F)C(F)(F)F)ccnc1CO
2-hydroxymethyl-3-methyl-4-(2,2,3,3,3-pentafluoropropoxy)-pyridine

ظروف التفاعل

درجة الحرارة
110°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزconcentrated
  2. 2
    workup.DISSOLUTIONThe residue was dissolved in methanol (30 ml)
  3. 3
    workup.ADDITION2N aqueous sodium hydroxide (20 ml) was added
  4. 4
    workup.STIRRINGthe mixture was stirred at room temperature for 2 hours
  5. 5
    تركيزAfter concentration, water
  6. 6
    workup.ADDITIONwas added to the residue
  7. 7
    استخلاصthe mixture was extracted with ethyl acetate
  8. 8
    تجفيفThe extract was dried over magnesium sulfate
  9. 9
    workup.DISTILLATIONthe solvent was then distilled off
  10. 10
    غسيلElution
  11. 11
    أخرىwith chloroform-methanol (10:1) and recrystallization from isopropyl ether

الإجراء التجريبي

Concentrated sulfuric acid (2 drops) was added to a solution of 2,3-dimethyl-4-(2,2,3,3,3-pentafluoropropoxy)-pyridine-1-oxide (2.5 g) in acetic anhydride (8 ml) and the mixture was stirred at 110° C. for 2 hours and then concentrated. The residue was dissolved in methanol (30 ml), 2N aqueous sodium hydroxide (20 ml) was added, and the mixture was stirred at room temperature for 2 hours. After concentration, water was added to the residue and the mixture was extracted with ethyl acetate. The extract was dried over magnesium sulfate, the solvent was then distilled off, and the residue was applied to a silica gel (50 g) column. Elution with chloroform-methanol (10:1) and recrystallization from isopropyl ether gave 1.6 g of 2-hydroxymethyl-3-methyl-4-(2,2,3,3,3-pentafluoropropoxy)-pyridine as a brown oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05639478uspto-grants-1997_06