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Hydrazine, dihydrochloride → HCID 15480333、化合物

HRID 1741255
ノート
印刷プレビュー

反応式

HRID 1741255 の反応式
[CH2:1]([CH:3]([C:11](=O)[C:12]1[C:17]([CH3:18])=[CH:16][C:15]([CH3:19])=[CH:14][C:13]=1[CH3:20])[C:4](=O)[C:5]([O:7][CH2:8][CH3:9])=[O:6])[CH3:2].Cl.Cl.[NH2:24][NH2:25]>CCO>[CH2:1]([C:3]1[C:11]([C:12]2[C:17]([CH3:18])=[CH:16][C:15]([CH3:19])=[CH:14][C:13]=2[CH3:20])=[N:24][NH:25][C:4]=1[C:5]([O:7][CH2:8][CH3:9])=[O:6])[CH3:2]
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

4

反応物 2

HCID 17548Hydrazine, dihydrochlorideHCID 15870414HCID 15870414、化合物

生成物 1

HCID 15480333HCID 15480333、化合物

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
80 °C

実験手順

A mixture of ethyl 3-ethyl-2,4-dioxo-4-(2,4,6trimethylphenyl)butanoate (6.0 g, 20.7 mmol) and hydrazine dihydrochloride (2.17 g, 20.7 mmoL) in 100 mL of EtOH was stirred at 80° C. for 6 hours. The solvent was then removed from the mixture. 200 mL of water was added to the residue and mixture was neutralized by the addition of solid NaHCO3. The product was extracted into ether. The ether extract was dried over Na2SO4 and evaporated to give 5.8 g as an oil which was used in the next reaction without farther purification.

後処理

  1. customThe solvent was then removed from the mixture
  2. addition200 mL of water was added to the residue and mixture
  3. additionwas neutralized by the addition of solid NaHCO3
  4. extractionThe product was extracted into ether
  5. extractionThe ether extract
  6. dry with materialwas dried over Na2SO4
  7. customevaporated
  8. customto give 5.8 g as an oil which
  9. customwas used in the next reaction without farther purification

出典と根拠

ORDレコード
ord-5616ef379a354c0facc65c10679039f9
出典データセット
uspto-grants-1999_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05973152

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート