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Ethanol → N-(Hex-5-en-1-yl)hex-5-en-1-amine

HRID 11440
ノート
印刷プレビュー

反応式

HRID 11440 の反応式
C(O)C.[OH-].[K+].[CH2:6]([N:12]([CH2:17][CH2:18][CH2:19][CH2:20][CH:21]=[CH2:22])CCC#N)[CH2:7][CH2:8][CH2:9][CH:10]=[CH2:11].O>C(Cl)(Cl)Cl>[CH2:6]([NH:12][CH2:17][CH2:18][CH2:19][CH2:20][CH:21]=[CH2:22])[CH2:7][CH2:8][CH2:9][CH:10]=[CH2:11]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 702EthanolHCID 962WaterHCID 14797Potassium HydroxideHCID 121366273-(Di-5-hexenyl)aminopropionitrile

生成物 1

HCID 15640332N-(Hex-5-en-1-yl)hex-5-en-1-amine収率 21%

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

実験手順

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

Next, ethanol (8.6 ml) and potassium hydroxide (0.85 g, 13 mmol) were added to 3-(di-5-hexenyl)aminopropionitrile (2.0 g, 8.6 mmol), and the mixture was refluxed for 7.5 hours. The reaction mixture was allowed to stand, and then water (150 ml) and chloroform (150 ml) were added to the reaction mixture. Layers were separated, and the organic layer was dried over sodium sulfate. The organic layer was concentrated under reduced pressure, and the residue was purified by basic silica gel column chromatography to give 0.32 g (21%) of the titled compound as a pale yellow oily matter.

後処理

  1. temperaturethe mixture was refluxed for 7.5 hours
  2. customLayers were separated
  3. dry with materialthe organic layer was dried over sodium sulfate
  4. concentrationThe organic layer was concentrated under reduced pressure
  5. customthe residue was purified by basic silica gel column chromatography

出典と根拠

ORDレコード
ord-9e54ec4ad8e845f3b4b1b6c76d7c398a
出典データセット
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07098226B2

反応ノート

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