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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45497Generated: October 30, 2026

4-(4-Bromophenyl)-4-hydroxypiperidine → 4-(4-Bromophenyl)-4-(4-chlorophenyl)piperidine

https://huagongshe.com/reaction/45497

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Bromophenyl)-4-hydroxypiperidineHCID 93911—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventChlorobenzeneHCID 7964—
Product4-(4-Bromophenyl)-4-(4-chlorophenyl)piperidineHCID 49760777203.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of 4-(4-Bromo-phenyl)-piperidin-4-ol (4.02 g, 15.7 mmol) in chlorobenzene (30 ml) was added dropwise to a suspension of aluminium chloride (7.32 g, 54.9 mmol) in chlorobenzene (10 ml) at 0° C. The reaction mixture was stirred at 0° C. for 2 hours, quenched by addition of ice then methyl t-butyl ether added. After stirring for 1 hour the precipitate was collected by filtration washed with water, methyl t-butyl ether and water to afford the title compound (5.59 g, 92% yield). LC/MS: (PS-B3) Rt 3.57 [M+H]+ 350, 352.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541461B2
Source datasetuspto-grants-2013_09
ORD IDord-071d2dbb8fcc4578991be19624694c5e
Source noteuspto-grants-2013_09