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Sodium hydride → (2E)-3-(2-ethyl-2H-indazol-4-yl)acrylonitrile

HRID 1639772
ノート
印刷プレビュー

反応式

HRID 1639772 の反応式
[C:1]([CH2:3]P(=O)(OCC)OCC)#[N:2].[H-].[Na+].[CH2:14]([N:16]1[CH:24]=[C:23]2[C:18]([CH:19]=[CH:20][CH:21]=[C:22]2[CH:25]=O)=[N:17]1)[CH3:15]>O1CCCC1.[Cl-].[NH4+]>[CH2:14]([N:16]1[CH:24]=[C:23]2[C:18]([CH:19]=[CH:20][CH:21]=[C:22]2/[CH:25]=[CH:3]/[C:1]#[N:2])=[N:17]1)[CH3:15]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 24758Sodium hydrideHCID 75676Diethyl (cyanomethyl)phosphonateHCID 593345522-ethyl-2H-indazole-4-carbaldehyde

生成物 1

HCID 59334569(2E)-3-(2-ethyl-2H-indazol-4-yl)acrylonitrile収率 93.8%

試薬・触媒・溶媒 2

HCID 8028Tetrahydrofuran溶媒2 回
HCID 25517
Ammonium Chloride
溶媒

反応条件

温度
0 °C

実験手順

To a solution of diethyl cyanomethylphosphonate (254 μL, 1.57 mmol) in tetrahydrofuran (6 mL) was added 60% sodium hydride (57.9 mg, 1.45 mmol) under ice-cooling, and the mixture was stirred at 0° C. for 15 min. To the mixture was added a solution of 2-ethyl-2H-indazole-4-carbaldehyde (210 mg, 1.20 mmol) in tetrahydrofuran (6 mL) under ice-cooling, and the mixture was stirred under ice-cooling for 15 min. The reaction solution was diluted with saturated aqueous ammonium chloride solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane=15/85→50/50) to give the title compound (222 mg, yield 93%).

後処理

  1. temperaturecooling
  2. temperaturecooling
  3. stirringthe mixture was stirred under ice-
  4. temperaturecooling for 15 min
  5. extractionthe mixture was extracted with ethyl acetate
  6. washThe extract was washed with saturated brine
  7. dry with materialdried over anhydrous sodium sulfate
  8. customthe solvent was evaporated under reduced pressure
  9. customThe residue was purified by silica gel column chromatography (ethyl acetate/hexane=15/85→50/50)

出典と根拠

ORDレコード
ord-bcbade188e9f45198606bf614c8ae2bf
出典データセット
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08110585B2

反応ノート

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