반응 #465940

ord-d56a9f234b74453eaae79dd95b7cda1e

반응 방정식

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

반응 조건

온도
110°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    농축concentrated
  2. 2
    workup.DISSOLUTIONThe residue was dissolved in methanol (30 ml)
  3. 3
    workup.ADDITION2 N aqueous sodium hydroxide (20 ml) was added
  4. 4
    workup.STIRRINGthe mixture was stirred at room temperature for 2 hours
  5. 5
    농축After concentration, water
  6. 6
    workup.ADDITIONwas added to the residue
  7. 7
    추출the mixture was extracted with ethyl acetate
  8. 8
    건조The extract was dried over magnesium sulfate
  9. 9
    workup.DISTILLATIONthe solvent was then distilled off
  10. 10
    세척Elution
  11. 11
    기타with chloroform-methanol (10:1) and recrystallization from isopropyl ether

실험 절차

Concentrated sulfuric acid (2 drops) was added to a solution 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), 2 N 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 te 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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06296875B1uspto-grants-2001_10