Isopropyl iodide → 2-(1-Isopropyl-1H-pyrazol-3-yl)ethanol

HRID 726340ノート

反応式

HRID 726340 の反応式
[NH:1]1[CH:5]=[CH:4][C:3]([CH2:6][CH2:7][OH:8])=[N:2]1.C(=O)([O-])[O-].[Na+].[Na+].I[CH:16]([CH3:18])[CH3:17]>CN(C)C=O>[CH:16]([N:1]1[CH:5]=[CH:4][C:3]([CH2:6][CH2:7][OH:8])=[N:2]1)([CH3:18])[CH3:17]

参加物

5

反応条件

温度
100 °C

実験手順

To a solution of 1.0 gm (9.0 mMol) 2-(3-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 micture 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.

後処理

  1. temperatureThe reaction micture was then cooled to ambient and
  2. concentrationthen concentrated under reduced pressure
  3. customThe residue was partitioned between water and dichloromethane
  4. washThe organic phase was then washed with water
  5. dry with materialwas then dried over sodium sulfate
  6. concentrationThe remaining organics were concentrated under reduced pressure

出典と根拠

ORDレコード
ord-d24d0525c05342cf873fc9b333be9b53
出典データセット
uspto-grants-1998_01
特許番号
US05708187

反応ノート

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