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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576526Generated: October 25, 2026

Dimethylformamide → 3-Allyl-1,3-dimethyl-piperidin-4-one

https://huagongshe.com/reaction/576526

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantAllyl bromideHCID 7841—
ReactantSodium hydrideHCID 24758—
Reactant1,3-Dimethyl-4-piperidoneHCID 107311—
Product3-Allyl-1,3-dimethyl-piperidin-4-oneHCID 13740022—

Reaction Steps

1,3-Dimethyl-piperidin-4-one (6 g, 47.24 mmol) was dissolved in DMF (20 mL) and sodium hydride (2.07 g, 51.95 mmol) was added portionwise at 0° C. under nitrogen atmosphere. This was followed by dropwise addition of allyl bromide (5.71 g, 47.19 mmol) in DMF (4 mL) at 0° C. under nitrogen atmosphere. The reaction mixture was stirred at RT for 15 min, quenched with ice-water and extracted with EtOAc (3×100 mL). The organic layer was washed with water (3×100 mL), dried over sodium sulfate and concentrated under reduced pressure. The residue was purified by column chromatography (silica gel, 100-200 mesh) eluting with 7% EtOAc in hexane to obtain 3.2 g of 3-allyl-1,3-dimethyl-piperidin-4-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040519B2
Source datasetuspto-grants-2015_05
ORD IDord-bfd8020827dd423b83dc1fc7f89d407d
Source noteuspto-grants-2015_05