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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651550Generated: October 26, 2026

2-Bromoethanol → 2-[4-[(4-Chlorophenyl)-2-pyridylmethoxy]-1-piperidyl]ethanol

https://huagongshe.com/reaction/1651550

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoethanolHCID 10898—
ReactantPotassium CarbonateHCID 11430—
Reactant2-((4-Chlorophenyl)(4-piperidinyloxy)methyl)pyridineHCID 11141197—
SolventAcetoneHCID 180—
Product2-[4-[(4-Chlorophenyl)-2-pyridylmethoxy]-1-piperidyl]ethanolHCID 1505585556%

Reaction Steps

1.00 g (3.30 mmol) of 4-[(4-chlorophenyl)-2-pyridylmethoxy]piperidine and 0.49 g (3.92 mmol) of 2-bromoethanol were dissolved in 10 ml of acetone, and 0.55 g (3.98 mmol) of potassium carbonate was added to the mixed solution. The mixture was stirred at room temperature for 15 hours. After the reaction, the insolubles were filtered off, and the filtrate was concentrated under reduced pressure. The residue was separated by silica gel column chromatography using a mixture of chloroform and methanol in the volume ratio 20:1 as the eluent. The desired fraction was concentrated under reduced pressure to give 0.64 g (56%) of 2-[4-[(4-chlorophenyl)-2-pyridylmethoxy]-1-piperidyl]ethanol as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04929618
Source datasetuspto-grants-1990_05
ORD IDord-ad93b1a26b8c4b6c87d82aafe320b6cc
Source noteuspto-grants-1990_05