반응 #1543044

ord-e533b185bc754ec9b41126b30609ce18

반응 방정식

N#CCBr
bromoacetonitrile
O=C([O-])[O-].[K+].[K+]
potassium carbonate
COC(=O)c1c(OCC#N)nc(C(F)(F)F)c(C(=O)OC)c1CC(C)C
dimethyl 2-(cyanomethoxy)-4-(2-methylpropyl)-6-(trifluoromethyl)-3, 5-pyridine-dicarboxylate
COC(=O)c1c(O)nc(C(F)(F)F)c(C(=O)OC)c1CC(C)C
dimethyl 2-hydroxy-4-(2-methylpropyl)-6-(trifluoromethyl)- 3, 5-pyridinedicarboxylate

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    여과suction filtered
  2. 2
    workup.ADDITIONThe filtrate was diluted with 400 mL of water
  3. 3
    추출extracted with four 50 mL portions of methylene chloride
  4. 4
    건조The combined extracts were dried with magnesium sulfate
  5. 5
    기타the solvent was removed by rotary evaporation

실험 절차

This example illustrates the preparation of Compound 80, namely, dimethyl 2-(cyanomethoxy)-4-(2-methylpropyl)-6-(trifluoromethyl)-3, 5-pyridine-dicarboxylate. A solution of 6.38 g (0.019 mol) of dimethyl 2-hydroxy-4-(2-methylpropyl)-6-(trifluoromethyl)- 3, 5-pyridinedicarboxylate (Compound 1) in 50 mL of dimethylformamide was prepared and to it was added 7.2 g (0.06 mol) of bromoacetonitrile and 8.3 g (0.06 mol) of anhydrous potassium carbonate. The mixture was stirred at room temperature overnight then suction filtered. The filtrate was diluted with 400 mL of water and extracted with four 50 mL portions of methylene chloride. The combined extracts were dried with magnesium sulfate and the solvent was removed by rotary evaporation giving 7.09 g (98.9% yield) of a dark amber oil. Silica gel chromatography with 10% ethyl acetate, 90% cyclohexane gave 3.51 g (49%) of Compound 80 as a clear colorless oil.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05843867uspto-grants-1998_12