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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278250Generated: October 30, 2026

1-Benzoylpiperidine-4-carbaldehyde → 4-(1-Hydroxy-prop-2-enyl)-1-benzoyl piperidine

https://huagongshe.com/reaction/278250

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzoylpiperidine-4-carbaldehydeHCID 15681284—
ReactantHCID 178418507HCID 178418507—
SolventTetrahydrofuranHCID 8028—
Product4-(1-Hydroxy-prop-2-enyl)-1-benzoyl piperidineHCID 1818759572.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 500 mg of 1-benzoylpiperidine-4-carboxaldehyde (Step C) in 10 mL THF at −78° C., was added 2.99 mmol of vinyl magnesium bromide. The solution was warmed to 0° C. and stirred for 1 h. The reaction was quenched with 15 mL of aq. ammonium chloride and extracted with 3×20 mL ether and the combined organic layers were dried over magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by flash chromatography with 2:1 hexane : ethyl acetate followed by 1:1 hexane:ethyl acetate followed by hexane:ethyl acetate:methanol, 50:50:5 to give 411 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06358979B1
Source datasetuspto-grants-2002_03
ORD IDord-9a23bd4604a54131891d87ad69aa1151
Source noteuspto-grants-2002_03