Acrylonitrile → N-(2-Cyanoethyl)glycine ethyl ester
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
Reactant 3
Product 1
Reagents, catalysts & solvents 1
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
- temperaturewhile heating
- stirringThe reaction mixture was stirred for 5 hours
- temperaturewith heating
- customthe organic layer was separated
- extractionThe aqueous layer was extracted with ethyl ether
- customas separated above
- dry with materialThe combined organic layer was dried over anhydrous magnesium sulfate
- filtrationfiltered
- concentrationThe filtrate was concentrated under reduced pressure
- customto remove the solvent
- 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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