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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35095Generated: October 26, 2026

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

https://huagongshe.com/reaction/35095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium hydrideHCID 24758—
Reactant1-(4-Nitrophenyl)-3-azabicyclo[3.1.1]heptane-2,4-dioneHCID 14872629—
SolventDimethylformamideHCID 6228—
Product3-Allyl-1-(4-nitrophenyl)-3-azabicyclo[3.1.1]heptane-2,4-dioneHCID 20027816—

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. 1.27 ml of allyl bromide 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 and, after concentration by evaporation and subsequent recrystallisation from ethyl acetate/petroleum ether, the product is obtained having a melting point of 146°-147°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04764640
Source datasetuspto-grants-1988_08
ORD IDord-005ccd7eff2e40209918864e552ec70b
Source noteuspto-grants-1988_08