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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | N-(2-Cyanoethyl)glycine ethyl ester | HCID 521172 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(2-Cyanoethyl)-N-formylglycine | HCID 19849818 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04868202 |
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| Source dataset | uspto-grants-1989_09 |
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| ORD ID | ord-3218ba32a7d74467a8304dfb5d1b1349 |
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| Source note | uspto-grants-1989_09 |
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