HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244425Generated: November 1, 2026
Dicyclohexylcarbodiimide → HCID 86606570, compound
https://huagongshe.com/reaction/2244425
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | 3-Methoxypropionic acid | HCID 134442 | — |
| Reactant | Ethyl 2-amino-2-cyanoacetate | HCID 288716 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86606570 | HCID 86606570 | 76% |
Reaction Steps
A solution of aminocyanacetic acid ethyl ester (1.00 g, 7.80 mmol) in ethyl acetate (16.00 ml) was cooled to 0° C. and treated with dimethylaminopyridine (0.09 g, 0.78 mmol) and dicyclohexylcarbodiimide (1.93 g, 9.36 mmol). 3-Methoxy-propionic acid (0.81 g, 7.80 mmol) was added portionwise. After completed addition, the mixture was stirred at 0° C. for 1 h) then at room temperature for 3 h. The precipitated dicyclohexylurea was filtered off and the mother liquors washed with water, dried over sodium sulphate and evaporated. The residue was purified by trituration in diisopropylether to yield cyano-(3-methoxy-propionylamino)-acetic acid ethyl ester (1.27 g, 76%), MS (ISP): m/e=215.3 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07678815B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-1e881876bffc4eee9e5e31b83cc9d282 |
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| Source note | uspto-grants-2010_03 |
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