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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727211Generated: October 31, 2026

(3-Bromopropyl)benzene → 1-[4-(3-Phenylpropoxy)-1-piperidinyl]ethanone

https://huagongshe.com/reaction/1727211

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Bromopropyl)benzeneHCID 12503—
ReactantSodium hydrideHCID 24758—
Reactant1-(4-Hydroxypiperidin-1-yl)ethan-1-oneHCID 10749291—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
SolventDimethylformamideHCID 6228—
Product1-[4-(3-Phenylpropoxy)-1-piperidinyl]ethanoneHCID 6905432327.4%

Reaction Steps

1-Acetylpiperidin-4-ol (Preparation 193, 8 g, 60 mmol) in N,N-dimethylformamide (50 ml) was added dropwise to a stirred suspension of sodium hydride (50% wt dispersion in oil, 3.68 g, 80 mmol) in N,N-dimethylformamide (50 ml) at room temperature under nitrogen. After stirring the reaction mixture for 4 hours, 1-bromo-3-phenylpropane (12.94 g, 65 mmol) in N,N-dimethylformamide (50 ml) was added dropwise to the solution at 0° C. and the reaction mixture was stirred for a further 4 h. The solution was diluted with isopropyl alcohol (20 ml) and water (100 ml) and then evaporated to give a semi solid. Water (100 ml) was added and the solution was extracted with petroleum ether (3×100 ml). The combined organic extracts were dried (Na2SO4) and concentrated in vacuo to give an orange oil (4.3 g, 27%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07494992B2
Source datasetuspto-grants-2009_02
ORD IDord-1d4a94d44e824426a692d6139dca7bda
Source noteuspto-grants-2009_02