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Ethyl Acetoacetate → HCID 10176552、化合物

HRID 325129
ノート
印刷プレビュー

反応式

HRID 325129 の反応式
[C:1]([O:7][CH2:8][CH3:9])(=[O:6])[CH2:2][C:3]([CH3:5])=[O:4].[H-].[Na+].Cl[CH2:13][CH:14]=[C:15]([CH3:17])[CH3:16]>CN(C)C=O>[CH2:8]([O:7][C:1](=[O:6])[CH:2]([C:3](=[O:4])[CH3:5])[CH2:13][CH:14]=[C:15]([CH3:17])[CH3:16])[CH3:9]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 8868Ethyl AcetoacetateHCID 104291-Chloro-3-methyl-2-buteneHCID 24758Sodium hydride

生成物 1

HCID 10176552HCID 10176552、化合物収率 58.4%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒2 回

実験手順

To a solution of 26.05 g ethyl acetoacetate in 150 ml of dimethylformamide, 8.30 g 60% sodium hydride were added portionwise over 1 hour while the temperature rose to 60° C. After cooling down to room temperature, a solution of 24.8 g 1-chloro-3-methyl-2-butene in 50 ml of dimethylformamide was dropped in. Then the mixture was stirred at room temperature for 2.5 hours. The mixture was quenched with water and extracted with ether. The combined organic phase was dried, filtered and evaporated to dryness. The resulting yellow oil was purified by distillation to yield 23.16 g of a colourless oil.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customrose to 60° C
  2. customThe mixture was quenched with water
  3. extractionextracted with ether
  4. customThe combined organic phase was dried
  5. filtrationfiltered
  6. customevaporated to dryness
  7. distillationThe resulting yellow oil was purified by distillation

出典と根拠

ORDレコード
ord-c3b38ae825f14c7f9e277aec2c5b6dad
出典データセット
uspto-grants-2001_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06222062B1

反応ノート

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