HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362153Generated: October 29, 2026
Acetamidomalonic acid diethyl ester → HCID 86753717, compound
https://huagongshe.com/reaction/362153
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetamidomalonic acid diethyl ester | HCID 14041 | — |
| Reactant | cis-Crotyl Bromide | HCID 5354843 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86753717 | HCID 86753717 | 98% |
Reaction Steps
4.37 g (190 mmol) of sodium metal were dissolved in 110 ml of anhydrousethanol. 41.14 g (189.6 mmol) of diethyl acetamidomalonate dissolved in 270ml of anhydrous ethanol were added and the mixture was heated under reflux for 10 minutes. 25.65 g (168 mmol) of (Z)-1-bromo-2-butene were added dropwise at room temperature and the mixture was stirred overnight, then evaporated to dryness under vacuum and the residue was partitioned betweenethyl acetate and 0.1M hydrochloric acid. The organic phase was washed withsaturated sodium hydrogen carbonate solution followed by saturated sodium chloride solution and dried over anhydrous magnesium sulphate. After removal of the solvent by evaporation the crude product was chromatographed on silica gel using 66% ethyl acetate in petroleum ether as eluent to obtain 44.69 g of diethyl (Z)-2-acetamido-2-(2-butenyl)malonate as a colourless oil;1H NMR (250 MHz, CDCl3) δ:1.2 (t, 6 H), 1.6 (d, 3 H), 2.0 (s, 3 H), 3.1 (d, 2 H), 4.2 (q, 4 H), 5.1(m, 1 H), 5.6 (m, 1 H), 6.7 (s, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05866684 |
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| Source dataset | uspto-grants-1999_02 |
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| ORD ID | ord-ebfaa796ecba432cafec97e28e27746f |
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| Source note | uspto-grants-1999_02 |
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