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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619309Generated: October 25, 2026

Allyl bromide → 3-Allyl-2-piperidinone

https://huagongshe.com/reaction/1619309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant2-PiperidoneHCID 12665—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product3-Allyl-2-piperidinoneHCID 13380374—

Reaction Conditions

Temperature-75 °C

Reaction Steps

To a solution of piperidin-2-one (0.5 g, 5.0 mmol, 1 equiv) in dry THF (10.0 mL) was added nBuLi (4.2 ml, 10.5 mmol, 2.1 equiv) dropwise at 0° C. The mixture was then cooled to −75° C. and excess 3-bromoprop-1-ene was added to the mixture. The reaction mixture was kept at −78° C. for 1 h, quenched with NH4Cl solution and extracted with ethyl acetate (3×20 mL). The combined organic layers were dried over Na2SO4 and concentrated under reduced pressure to give the desired product, which was directly used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772301B2
Source datasetuspto-grants-2014_07
ORD IDord-4ca40d76344443dcac5825a2dc766950
Source noteuspto-grants-2014_07