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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427437Generated: October 30, 2026

Water → HCID 18357115, compound

https://huagongshe.com/reaction/427437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant4-Bromobenzyl bromideHCID 68527—
Reactant1-(4-Pyridyl)piperazineHCID 70517—
SolventDimethylformamideHCID 6228—
ProductHCID 18357115HCID 1835711529.8%

Reaction Steps

A solution of N-(4-pyridyl)piperazine (0.33 g) in dry dimethylformamide (15 ml) was treated with sodium hydride (0.14 g) (45-55% dispersion in oil). The reaction mixture was then stirred for 45 minutes at ambient temperature under argon. 4-Bromobenzyl bromide (0.58 g) was added and the mixture heated slowly to 60° C. and then maintained at this temperature for 2 hours. The resulting mixture was then poured into water, basified with aq.NaHCO3 solution and then extracted with diethyl ether. The organic extracts were then washed with aq.NaHCO3, water, brine, dried (Na2SO4) and evaporated. The residue was recrystallised from acetonitrile to give 1-(4-pyridyl)-4-(4-bromobenzyl)piperazine (0.2 g) as a solid, m.p. 140-141° C.; microanalysis, found: C,55.3; H,5.2; N,12.0%; C16H18N3Br requires: C,55.4; H,5.7; N,12.1%; NMR: (CDCl3) 2.54(t,4H); 3.2(t,4H); 3.51(s,2H); 6.66(d,2H); 7.23(d,2H); 7.46(d,2H); 8.29(d,2H); MS: m/z 332 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313127B1
Source datasetuspto-grants-2001_11
ORD IDord-ce13ed36ea2f4faeae2a8a7eba8699ac
Source noteuspto-grants-2001_11