HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362150Generated: October 25, 2026
Acetamidomalonic acid diethyl ester → diethyl (E)-2-acetamido-2-(2-butenyl)malonate
https://huagongshe.com/reaction/362150
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetamidomalonic acid diethyl ester | HCID 14041 | — |
| Reactant | 2-Butene, 1-bromo-, (2E)- | HCID 637532 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | diethyl (E)-2-acetamido-2-(2-butenyl)malonate | HCID 86753714 | 87.8% |
Reaction Steps
3.86 g (168 mmol) of sodium metal were dissolved in 106 ml of anhydrousethanol. 36.35 g (168 mmol) of diethyl acetamidomalonate dissolved in 225 ml of anhydrous ethanol were added and the mixture was heated under refluxfor 10 minutes. 22.66 g (168 mmol) of (E)-1-bromo-2-butene were added dropwise at room temperature and the mixture was stirred overnight and then evaporated to dryness under a vacuum. The residue was partitioned between ethyl acetate and 0.1M hydrochloric acid. The organic phase was washed with saturated sodium hydrogen carbonate solution and then with saturated sodium chloride solution and dried over anhydrous magnesium sulphate. The solvent was evaporated to give 40 g of diethyl (E)-2-acetamido-2-(2-butenyl)malonate as a colourless oil; 1H NMR (250 MHz, CDCl3) δ: 1.25 (t, 6 H), 1.6 (d, 3 H), 2.0 (s, 3 H), 2.9 (d, 2 H), 4.2 (q, 4 H), 5.15 (m, 1 H) 5.5 (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-d0b36201542649e09c8e188c5f1a57f7 |
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| Source note | uspto-grants-1999_02 |
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