Acrylonitrile → N-(2-Cyanoethyl)glycine ethyl ester

HRID 1737398Notes

Reaction equation

HRID 1737398 reaction equation
Cl.[CH2:2]([O:4][C:5](=[O:8])[CH2:6][NH2:7])[CH3:3].[OH-].[K+].[C:11](#[N:14])[CH:12]=[CH2:13]>O>[CH2:2]([O:4][C:5](=[O:8])[CH2:6][NH:7][CH2:13][CH2:12][C:11]#[N:14])[CH3:3]

Participants

5

Conditions

Temperature
55 °C

Procedure

139.6 g (1 mole) of glycine ethyl ester hydrochloride was dissolved in 80 ml of distilled water and to this solution was added 230 ml of an aqueous solution of 67.3 g (1.2 mole eq.) of potassium hydroxide. Then, 106.2 g (2 mole eq.) of acrylonitrile was added to the reaction solution while heating and stirring at 50 to 60° C. The reaction mixture was stirred for 5 hours with heating and then the organic layer was separated. The aqueous layer was extracted with ethyl ether and the extract was combined with the organic layer as separated above. The combined organic layer was dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure to remove the solvent. The residue was distilled under reduced pressure (100 to 150° C./10.25 Storr) to obtain 65.6 g (Yield: 48 %) of the title compound.

Workup

  1. temperaturewhile heating
  2. stirringThe reaction mixture was stirred for 5 hours
  3. temperaturewith heating
  4. customthe organic layer was separated
  5. extractionThe aqueous layer was extracted with ethyl ether
  6. customas separated above
  7. dry with materialThe combined organic layer was dried over anhydrous magnesium sulfate
  8. filtrationfiltered
  9. concentrationThe filtrate was concentrated under reduced pressure
  10. customto remove the solvent
  11. distillationThe residue was distilled under reduced pressure (100 to 150° C./10.25 Storr)

Sources & evidence

ORD record
ord-e6347e70a70f413fa1b517f39b2de681
Source dataset
uspto-grants-1999_10
Patent number
US05962468

Reaction notes

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