HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779769Generated: October 25, 2026
Acetamidomalonic acid diethyl ester → 2-(Acetylamino)-2-[4-(acetyloxy)butyl]propanedioic acid, diethyl ester
https://huagongshe.com/reaction/1779769
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetamidomalonic acid diethyl ester | HCID 14041 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Butanol, 4-bromo-, 1-acetate | HCID 78491 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(Acetylamino)-2-[4-(acetyloxy)butyl]propanedioic acid, diethyl ester | HCID 10544484 | 98.3% |
Reaction Steps
A stirred suspension of 95% sodium hydride (60.8 g, 2.532 mol) in anhydrous dimethylformamide (500 ml) under an atmosphere of argon was cooled to 0° C. (ice bath). A solution of diethyl acetamidomalonate (500 g, 2.302 mol) in anhydrous dimethylformamide (1.2 l) was added over a period of 45 minutes while keeping the reaction temperature below 18° C. After the addition was complete, the turbid solution was gradually warmed to room temperature. After stirring for one hour at room temperature, 4-bromobutyl acetate (471.5 g, 2.417 mol) was added. The mixture was then stirred at 59°-60° C. for 18 hours. The resulting slurry was cooled to room temperature, quenched with absolute ethanol (40 ml) and glacial acetic acid (4 ml), stirred for about 15 minutes, poured into a 10% lithium chloride solution and extracted with ethyl acetate (2×3 l). The combined ethyl acetate extracts were washed with 10% lithium chloride (3×3 l), dried (anhydrous sodium sulfate), and evaporated in vacuo to give 750 g of title product as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05627278 |
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| Source dataset | uspto-grants-1997_05 |
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| ORD ID | ord-edd2b570d0614d16890a97de4e799d03 |
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| Source note | uspto-grants-1997_05 |
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