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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789742Generated: November 2, 2026

Benzyl Bromide → 1-Benzyl-3-ethylpiperazine

https://huagongshe.com/reaction/1789742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactant2-EthylpiperazineHCID 14094188—
SolventDimethylformamideHCID 6228—
Product1-Benzyl-3-ethylpiperazineHCID 2203654170.3%

Reaction Steps

Benzyl bromide (38.7 g, 0.22 mol) was added in portions to an ice cold (˜0° C.) solution of 2-ethylpiperazine (25 g, 0.22 mol) in DMF (150 mL) with such a rate that the temperature did not exceed 20° C. The mixture was stirred for 1 h, the solvent was evaporated and the residue was partitioned between CHCl3/0.5 M HCl. The aqueous phase was made alkaline (11M NaOH) and extracted three times with CHCl3. The combined organic phases were dried (MgSO4) and concentrated. The resulting oil was purified by column chromatography on silica using CHCl3, followed by CHCl3/MeOH/NH4OH (95:5:0.3) as eluents to give 31.6 g (70%) of the title compound as a yellowish oil. Anal. (C13H20N2) H, N; C: calc, 76.42 found 75.85; H, N.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071180B2
Source datasetuspto-grants-2006_07
ORD IDord-281c91867e344a1896f5d9a576cd628a
Source noteuspto-grants-2006_07