HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477205Generated: October 26, 2026
Dicyclohexylcarbodiimide → HCID 15053735, compound
https://huagongshe.com/reaction/477205
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Formylglycine | HCID 75606 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Propanedioic acid, 2-amino-, 1,3-diethyl ester, hydrochloride (1:1) | HCID 3084143 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 15053735 | HCID 15053735 | 79.4% |
Reaction Steps
Diethyl 2-aminomalonate hydrochloride (4.2 g), formylglycine (2.3 g) and 1-hydroxybenzotriazole (2.7 g) are dissolved in dimethylformamide (50 ml). To the solution are added N,N'-dicyclohexylcarbodiimide (4.33 g) and triethylamine (2.12 g) at 0° to 5° C. The mixture is stirred at the same temperature for 2 hours and at room temperature for 15 hours. The reaction mixture is concentrated under reduced pressure. To the residue is added ethyl acetate, and the mixture is filtered to remove insoluble materials. The filtrate is washed, dried and evaporated to remove the solvent. The residue is purified by silica gel column chromatography [solvent; chloroform-ethyl acetate (1:5)]to give diethyl 2-[(N-formylglycyl)amino]malonate (4.1 g), m.p. 95°-96° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04886894 |
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| Source dataset | uspto-grants-1989_12 |
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| ORD ID | ord-ea779bf209574b1b9b9e2b0f4389dc5b |
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| Source note | uspto-grants-1989_12 |
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