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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647884Generated: November 1, 2026

1-Benzylpiperazine → HCID 67806111, compound

https://huagongshe.com/reaction/1647884

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BenzylpiperazineHCID 75994—
Reactant2-(4-Benzylpiperazin-1-yl)ethan-1-amineHCID 2735331—
Reactant2-Bromoethylamine hydrobromideHCID 2774217—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 60657227HCID 60657227—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTriethylamineHCID 8471—
ProductHCID 67806111HCID 67806111—

Reaction Steps

8.2 g of 4-chloro-3-nitro-benzoic acid-[N-(2-carboxy-ethyl)-amide](prepared from 4-chloro-3-nitro-benzoylchloride and β-alanine-methylester and subsequent saponification with 48% hydrobromic acid), 6.6 g of 2-(4-benzyl-piperazino)-ethylamine (prepared from 1-benzyl-piperazine and 2-bromo-ethylamine-hydrobromide in ethanol with the addition of potassium tert.butoxide), 4.2 ml of triethylamine and 25 ml of water are heated over a steam bath for 8 hours. The mixture is evaporated down and purified by column chromatography (silica gel; methylene chloride/methanol/glacial acetic acid=8:2:0.1 to 2:1:0.1). Yield: 9.2 g (67% of theory), Rf value: 0.47 (silica gel; methylene chloride/methanol/conc. ammonia=8:2:0.1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05434150
Source datasetuspto-grants-1995_07
ORD IDord-e2d652484b2e46299f0ffd3fb44fc75f
Source noteuspto-grants-1995_07