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Hydrazine hydrate (1:1) → HCID 54417124、化合物

HRID 2396904
ノート
印刷プレビュー

反応式

HRID 2396904 の反応式
[CH2:1]([C:3](=[CH:18][CH:19]([CH3:21])[CH3:20])[CH:4]=[CH:5][CH2:6][N:7]1C(=O)C2=CC=CC=C2C1=O)[CH3:2].O.NN>C(O)C>[CH2:1]([C:3](=[CH:18][CH:19]([CH3:20])[CH3:21])[CH:4]=[CH:5][CH2:6][NH2:7])[CH3:2]
参加物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 24654Hydrazine hydrate (1:1)HCID 54211318HCID 54211318、化合物

生成物 1

HCID 54417124HCID 54417124、化合物

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

A mixture of N-(4-ethyl-6-methyl-2,4-heptadiene-1-yl)phthalimide (17.62 g), hydrazine monohydrate (9.9 g), and ethanol (700 ml) was refluxed for 90 minutes under nitrogen atmosphere. The reaction mixture was evaporated in vacuo. The residue was dissolved in 10% aqueous potassium carbonate solution and extracted with ethyl acetate. The organic extract was washed with brine, dried over anhydrous magnesium sulfate, and evaporated to give 4-ethyl-6-methyl-2,4-heptadiene-1-ylamine as an oil.

後処理

  1. temperaturewas refluxed for 90 minutes under nitrogen atmosphere
  2. customThe reaction mixture was evaporated in vacuo
  3. dissolutionThe residue was dissolved in 10% aqueous potassium carbonate solution
  4. extractionextracted with ethyl acetate
  5. extractionThe organic extract
  6. washwas washed with brine
  7. dry with materialdried over anhydrous magnesium sulfate
  8. customevaporated

出典と根拠

ORDレコード
ord-20db761e03f74cfb808683b698074923
出典データセット
uspto-grants-1996_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05495023

反応ノート

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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