反応 #1543044

ord-e533b185bc754ec9b41126b30609ce18

反応方程式

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

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

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

実験手順

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.

出典

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