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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1950012Generated: November 2, 2026

Water → HCID 23087452, compound

https://huagongshe.com/reaction/1950012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(2-Chloroethyl)piperidineHCID 74827—
Reactant4-Bromonaphthalen-1-olHCID 575609—
SolventDimethylformamideHCID 6228—
ProductHCID 23087452HCID 2308745296.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 4-bromonaphthalen-1-ol (1.1 g) in N,N-dimethylformamide (30 ml) were sequentially added potassium carbonate (1.0 g) and 1-(2-chloroethyl)piperidine (1.1 g), and the solution was stirred for 1 hour at 60° C. Water was added thereto followed by stirring, the solution was extracted with ethyl acetate, then sequentially washed with water and brine, dried over anhydrous magnesium sulfate, and the solvent was then evaporated in vacuo. The residue was purified by NH silica gel column chromatography (hexane-ethyl acetate system) to obtain 1-[2-(4-bromonaphthalen-1-yloxy)ethyl]piperidine (1.59 g). This compound (800 mg) was used according to an analogous synthetic method to Preparation Example 51 to provide the title compound (518 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399520B2
Source datasetuspto-grants-2013_03
ORD IDord-434446266be04cf98033389a17b871d0
Source noteuspto-grants-2013_03