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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607907Generated: October 30, 2026

Formic Acid → N-(2-Cyanoethyl)-N-formylglycine

https://huagongshe.com/reaction/1607907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
ReactantN-(2-Cyanoethyl)glycine ethyl esterHCID 521172—
SolventEthanolHCID 702—
ProductN-(2-Cyanoethyl)-N-formylglycineHCID 19849818—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 21.0 g of N-(2-cyanoethyl)-glycine ethyl ester and 18.3 g of formic acid is refluxed for 2 h. After concentration of this mixture underreduced pressure, the residue is taken up in 50 ml of ethanol, and cooled to 0° C.; there is then added dropwise a solution of 25.5 g of potassium hydroxide and 40 ml of water in 80 ml of ethanol. After the reaction solution has warmed up to room temperature, the solvent is evaporated off, and the residue is acidified to pH 1 with conc. hydrochloric acid. The mixture is saturated with sodium chloride and subsequently extracted with ethyl acetate. The combined organic extracts are concentrated by evaporation to thus obtain N-(2-cyanoethyl)-N-formylglycine, m.p. 112°-114° C. (compound No. 1.1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04868202
Source datasetuspto-grants-1989_09
ORD IDord-3218ba32a7d74467a8304dfb5d1b1349
Source noteuspto-grants-1989_09