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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetamidomalonic acid diethyl esterHCID 14041—
Reactant2-Butene, 1-bromo-, (2E)-HCID 637532—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
Productdiethyl (E)-2-acetamido-2-(2-butenyl)malonateHCID 8675371487.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05866684
Source datasetuspto-grants-1999_02
ORD IDord-d0b36201542649e09c8e188c5f1a57f7
Source noteuspto-grants-1999_02