反应 #1543044

ord-e533b185bc754ec9b41126b30609ce18

反应方程式

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

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    过滤suction filtered
  2. 2
    workup.ADDITIONThe filtrate was diluted with 400 mL of water
  3. 3
    萃取extracted with four 50 mL portions of methylene chloride
  4. 4
    干燥The combined extracts were dried with magnesium sulfate
  5. 5
    其他the solvent was removed by rotary evaporation

实验过程

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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05843867uspto-grants-1998_12