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

HRID 18383
ノート
印刷プレビュー

反応式

HRID 18383 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 obtained mixture was refluxed for 7.5 hours. The reaction mixture was allowed to stand, then water (150 ml) and chloroform (150 ml) were added to the reaction mixture. After separation, the organic layer was dried over sodium sulfate and concentrated under reduced pressure, and the resulting residue was purified by basic silica gel column chromatography to give the target compound (0.32 g, 21%) as a pale yellow oily matter.

後処理

  1. temperaturethe obtained mixture was refluxed for 7.5 hours
  2. customAfter separation
  3. dry with materialthe organic layer was dried over sodium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customthe resulting residue was purified by basic silica gel column chromatography

出典と根拠

ORDレコード
ord-83150b480f524dde80da8571a47199d3
出典データセット
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07741346B2

反応ノート

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