反応 #452426

ord-9b1f852a20544f969f0f2f8380e9970a

反応方程式

CC(C)I
2-iodopropane
OCCc1cn[nH]c1
2-(4-pyrazolyl)-1-ethanol
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
CC(C)n1cc(CCO)cn1
title compound
収率 26.0%
CC(C)n1cc(CCO)cn1
2-(1-isopropyl-1H-pyrazol-4-yl)-1-ethanol
収率 26.0%

反応条件

温度
100°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度The reaction mixture was then cooled to ambient and
  2. 2
    濃縮then concentrated under reduced pressure
  3. 3
    その他The residue was partitioned between water and dichloromethane
  4. 4
    洗浄The organic phase was then washed with water
  5. 5
    乾燥was then dried over sodium sulfate
  6. 6
    濃縮The remaining organics were concentrated under reduced pressure

実験手順

To a solution of 1.0 gm (9.0 mMol) 2-(4-pyrazolyl)-1-ethanol in 36 mL dimethylformamide were added 2.38 gm (22.5 mMol) sodium carbonate followed by the dropwise addition of a solution of 0.89 mL (9.0 mMol) 2-iodopropane in 8 mL dimethylformamide. The reaction mixture was heated to 100° C. for 18 hours. The reaction mixture was then cooled to ambient and then concentrated under reduced pressure. The residue was partitioned between water and dichloromethane. The organic phase was then washed with water followed by saturated aqueous sodium chloride and was then dried over sodium sulfate. The remaining organics were concentrated under reduced pressure to give 0.36 gm (26.0%) of the title compound as a brown oil.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06126932uspto-grants-2000_10