Acetic Acid → n,n-Bis(2-cyanoethyl)octadecylamine

HRID 74713

反応式

HRID 74713 の反応式
[C:1](#[N:4])[CH:2]=[CH2:3].[CH2:5](O)[CH3:6].[CH2:8]([NH2:26])[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25].O.[NH3:28].[C:29](O)(=O)C>O>[C:29]([CH2:5][CH2:6][N:26]([CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25])[CH2:3][CH2:2][C:1]#[N:4])#[N:28]

参加物

7

反応物 5

HCID 176Acetic AcidHCID 702EthanolHCID 7855AcrylonitrileHCID 15793OctadecylamineHCID 12896473Azane;hydrate

生成物 1

HCID 10872492n,n-Bis(2-cyanoethyl)octadecylamine

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
77 °C

実験手順

40.2 g of acrylonitrile was added dropwise to an ethanol solution (150 ml) of 41.7 g of stearylamine at room temperature over 0.5 hours, 22.5 g of acetic acid was added dropwise thereto over 0.5 hours, and then stirred at 77° C. for 10 hours. After standing to cool to room temperature, the mixed solution was added with 200 ml of water and 22.8 g of 28% ammonia water, and extracted with 500 ml of ethyl acetate. The organic layer was separated from the solution, washed twice with 100 ml of water and 50 ml of saturated saline, dried over anhydrous magnesium sulfate. After distilling off the solvent, the concentrated residue was recrystallized using isopropyl alcohol as a solvent to obtain 42.4 g of a target compound as a white solid.

後処理

  1. temperatureto cool to room temperature
  2. extractionextracted with 500 ml of ethyl acetate
  3. customThe organic layer was separated from the solution
  4. washwashed twice with 100 ml of water and 50 ml of saturated saline
  5. dry with materialdried over anhydrous magnesium sulfate
  6. distillationAfter distilling off the solvent
  7. customthe concentrated residue was recrystallized

出典と根拠

ORDレコード
ord-d2fb62cec9164f48957a19e44449b09d
出典データセット
uspto-grants-2014_09
特許番号
US08830811B2

関連ノート

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