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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74765Generated: October 25, 2026

Ethyl acetamidocyanoacetate → Ethyl (acetylamino)(bicyclo[4.2.0]octa-1,3,5-trien-7-yl)cyanoacetate

https://huagongshe.com/reaction/74765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl acetamidocyanoacetateHCID 95422—
Reactant7-Bromobicyclo[4.2.0]octa-1,3,5-trieneHCID 568591—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
ProductEthyl (acetylamino)(bicyclo[4.2.0]octa-1,3,5-trien-7-yl)cyanoacetateHCID 8668573995.2%

Reaction Steps

Sodium (464 mg, 20.2 mmol, 1.2 eq.) was allowed to react with absolute ethanol (40 mL, 0.42 M); to the resulting mixture was added ethyl 2-(acetylamino)-2-cyanoacetate (3.44 g, 20.2 mmol, 1.2 eq.). After 20 minutes at 60° C., 7-bromobicyclo[4.2.0]octa-1,3,5-triene (3.092 g, 16.89 mmol, 1 eq.) was added and the reaction mixture was heated at reflux overnight, then filtered and concentrated in vacuo. The residue was diluted with water and extracted with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate, filtered, and concentrated in vacuo to give a dark oil, which was purified by silica gel chromatography (Gradient: 0% to 50% ethyl acetate in heptane) to give #99 (4.38 g) as a yellow gum. LC-MS: m/z 273.2 [M+H+], retention time=2.36 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08828401B2
Source datasetuspto-grants-2014_09
ORD IDord-1049b729081445a9a898331059c3b8f8
Source noteuspto-grants-2014_09