HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903598Generated: October 30, 2026
Acetamidomalonic acid diethyl ester → HCID 13105387, compound
https://huagongshe.com/reaction/1903598
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetamidomalonic acid diethyl ester | HCID 14041 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 20449793 | HCID 20449793 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13105387 | HCID 13105387 | — |
Reaction Steps
In 100 ml of ethanol was dissolved 3.4 g of sodium, and following addition of 32 g of diethyl acetylaminomalonate, the mixture was refluxed for 2 hours. To the reaction mixture was added dropwise a solution of 16.5 g of ethyl 2-bromosuccinamate in ethanol (40 ml) and under stirring the mixture was refluxed for 30 minutes. This reaction mixture was concentrated under reduced pressure, followed by addition of ethyl acetate and water, and stirred. The aqueous layer was separated and the ethyl acetate layer was extracted with water. These aqueous extracts were combined, washed with ethyl acetate, adjusted to pH 1.5 with conc. hydrochloric acid and extracted with ethyl acetate. The extract was washed with water, dried over anhydrous sodium sulfate and concentrated under reduced pressure. To the residue was added ethyl ether and the mixture was allowed to stand in a refrigerator, whereupon crystals separated out. Yield 7.3 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04436918 |
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| Source dataset | uspto-grants-1984_03 |
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| ORD ID | ord-8bd0a6b61da34f6ca280d959ad2bf4f8 |
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| Source note | uspto-grants-1984_03 |
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