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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505923Generated: November 1, 2026

Potassium Carbonate → cis-1-(4-Bromobenzyl)-3,5-dimethylpiperidine

https://huagongshe.com/reaction/1505923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromobenzyl bromideHCID 68527—
Reactant(3S,5S)-3,5-dimethylpiperidineHCID 7058087—
SolventTetrahydrofuranHCID 8028—
Productcis-1-(4-Bromobenzyl)-3,5-dimethylpiperidineHCID 5826670335.4%

Reaction Steps

A suspension of 4-bromobenzyl bromide (4.0 g, 16.0 mmol), cis, trans-(3,5-dimethylpiperidine) (1.81 g, 16.0 mmol) and potassium carbonate (2.65 g, 19.2 mmol) in THF (160 mL) was heated under reflux for 24 h. The reaction mixture was allowed to cool to ambient temperature, the solid removed by filtration and the filtrate evaporated in vacuo. The resultant residue was loaded onto a 50 g SCX-2 cartridge which was washed with methanol then eluted with 2N ammonia in methanol. Concentration of the combined basic fractions in vacuo followed by flash chromatography of the resultant residue (silica, 330 g column, ISCO, 0-25% ethyl acetate in pentane) afforded cis-1-(4-bromobenzyl)-3,5-dimethylpiperidine (1.60 g, 35%) as a colourless oil. 1H NMR (CDCl3, 300 MHz): 7.47-7.39 (m, 2H); 7.20 (d, J=8.0 Hz, 2H); 3.42 (s, 2H); 2.82-2.71 (m, 2H); 1.76-1.61 (m, 4H); 1.51-1.37 (m, 2H); 0.82 (d, J=6.4 Hz, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216980B2
Source datasetuspto-grants-2015_12
ORD IDord-e57691bc1b5e45b093ecd71e34c04123
Source noteuspto-grants-2015_12