Acetone → Glycine, N,N-bis(2-cyanoethyl)- (8CI)(9CI)

HRID 557989ノート

反応式

HRID 557989 の反応式
[NH2:1][CH2:2][C:3]([OH:5])=[O:4].C[N+:7]([CH3:10])(C)C.[OH-].[C:12](#[N:15])[CH:13]=[CH2:14].Cl.[CH3:17][C:18](C)=O>O>[C:12]([CH2:13][CH2:14][N:1]([CH2:17][CH2:18][C:10]#[N:7])[CH2:2][C:3]([OH:5])=[O:4])#[N:15]

参加物

7

反応条件

温度
10 °C

実験手順

Glycine (5 g, 67 mmol) was suspended in water (10 cm3) and TMAH (25% in water, 24.3 g, 67 mmol) was added slowly, keeping the temperature at <30° C. with an ice-bath. The mixture was then cooled to 10° C. and acrylonitrile (7.78 g, 146 mmol) was added. The mixture was stirred overnight, and allowed to warm to room temperature slowly. It was then heated at 50° C. for 2 hours, using a reflux condenser. After cooling with ice, the mixture was neutralized with HCl (6M, 11.1 cm3) and concentrated to a viscous oil. This was dissolved in acetone (100 cm3) and filtered to remove NMe4Cl. The filtrate was concentrated under reduced pressure to give an oil that was treated once more with acetone (100 cm3) and filtered to remove more NMe4Cl. Concentration of the filtrate gave 2-(bis(2-cyanoethyl)amino)acetic acid (11.99 g, 99.3%) as a colorless, viscous oil that crystallized over 1 week at room temperature to give a solid product, mp 73° C. (lit mp 77.8-78.8° C. Duplicate 13C signals indicate a partly zwitterionic form in CDCl3 solution.

後処理

  1. customat <30° C.
  2. temperatureto warm to room temperature slowly
  3. temperatureIt was then heated at 50° C. for 2 hours
  4. temperatureAfter cooling with ice
  5. concentrationconcentrated to a viscous oil
  6. dissolutionThis was dissolved in acetone (100 cm3)
  7. filtrationfiltered
  8. customto remove NMe4Cl
  9. concentrationThe filtrate was concentrated under reduced pressure
  10. customto give an oil that
  11. filtrationfiltered
  12. customto remove more NMe4Cl

出典と根拠

ORDレコード
ord-8f40545ac2014e149f09942f99f37b25
出典データセット
uspto-grants-2011_11
特許番号
US08062429B2

反応ノート

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