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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490329Generated: October 30, 2026

4-Bromobenzyl bromide → 1-[(4-Bromophenyl)methyl]piperidin-4-amine

https://huagongshe.com/reaction/490329

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromobenzyl bromideHCID 68527—
Reactant4-(N-Boc-amino)piperidineHCID 723833—
SolventDichloromethaneHCID 6344—
SolventDiisopropylethylamineHCID 81531—
Product1-[(4-Bromophenyl)methyl]piperidin-4-amineHCID 2331245687.8%

Reaction Steps

To a solution of 4-bromo benzylbromide (1.0 g, 4.1 mmol) in dichloromethane (20 ml) and diisopropyletylamine (1 ml) was added tert-butyl 4-piperidinylcarbamate (1.0 g, 5.0 mmol). The solution was then stirred at room temperature over night. The solvent was evaporated and 25 ml of 50% TFA in dichloromethane was added to the resulting white solid. The mixture was then stirred at room temperature for 2 h and then evaporated to dryness. The resulting solid was dissolved in water and extracted with toluene. After removal of the toluene the water phase was made basic with 1M NaOH giving a pH of 13. The water phase was then extracted with dichloromethane 3 times and the combined extracts were dried and then evaporated to give the pure product as a slightly yellow oil (0.96 g, 3.6 mmol)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528156B2
Source datasetuspto-grants-2009_05
ORD IDord-05781c454d734c16a82b7b62dcde2f08
Source noteuspto-grants-2009_05