Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 590618Generated: October 26, 2026

Water → 4-(4-Bromobenzyl)piperazine, N1-BOC protected

https://huagongshe.com/reaction/590618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromobenzyl bromideHCID 68527—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventDimethylformamideHCID 6228—
Product4-(4-Bromobenzyl)piperazine, N1-BOC protectedHCID 2795519—

Reaction Steps

To a mixture of 4-bromobenzyl bromide (5 g, 20 mmol) and N-Boc piperazine (4.47 g, 24 mmol) in DMF (25 mL), K2CO3 (5.52 g, 40 mmol) was added and the reaction mixture was stirred for 16 h at room temperature. After completion of reaction (monitored by TLC), the reaction mixture was poured into water (100 mL) and extracted with ethyl acetate (30 mL×3). The combined organic layers were washed with brine (100 mL), dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure to give crude product, V-1-I. This compound was used for next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233983B2
Source datasetuspto-grants-2016_01
ORD IDord-e3ebb349442a4dd5aa70e6b1b19bfef6
Source noteuspto-grants-2016_01