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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722865Generated: October 27, 2026

Iodoethane → 3-Ethyl-1-(4-nitrophenyl)-3-azabicyclo[3.1.1]heptane-2,4-dione

https://huagongshe.com/reaction/1722865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
Reactant1-(4-Nitrophenyl)-3-azabicyclo[3.1.1]heptane-2,4-dioneHCID 14872629—
ReactantEthyl acetate hexaneHCID 21226206—
SolventDimethylformamideHCID 6228—
Product3-Ethyl-1-(4-nitrophenyl)-3-azabicyclo[3.1.1]heptane-2,4-dioneHCID 20027840—

Reaction Steps

0.36 g of sodium hydride is added to a solution of 2.46 g of 1-(4-nitrophenyl)-3-azabicyclo[3.1.1]heptane-2,4-dione in 25 ml of N,N-dimethylformamide and the whole is stirred at room temperature for 30 minutes. 2.33 g of ethyl iodide dissolved in 10 ml of N,N-dimethylformamide are then added dropwise thereto. When the reaction is complete, the reaction mixture is freed of N,N-dimethylformamide. The residue is partitioned between ethyl acetate and water, and the organic phase is dried over magnesium sulphate, after concentration of evaporation, the product is obtained in the form of a solid. Melting point 175°-179°. Rf (ethyl acetate/hexane 4:1)=0.52.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04857660
Source datasetuspto-grants-1989_08
ORD IDord-315c6aafa31e417db85bb5fca6ee8f76
Source noteuspto-grants-1989_08