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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403110Generated: October 30, 2026

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

https://huagongshe.com/reaction/2403110

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantHydrochloric AcidHCID 313—
ReactantGlycineHCID 750—
ReactantAcrylonitrileHCID 7855—
ReactantTetramethylammonium hydroxideHCID 60966—
SolventWaterHCID 962—
ProductGlycine, N,N-bis(2-cyanoethyl)- (8CI)(9CI)HCID 8052399.3%

Reaction Conditions

Temperature10 °C

Reaction Steps

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 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 colourless, viscous oil that crystallised 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802609B2
Source datasetuspto-grants-2014_08
ORD IDord-4d9eda99154f4836a7562e7b03be3e46
Source noteuspto-grants-2014_08