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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 883571Generated: October 30, 2026

Acetic Acid → 1-(3-Chloro-4-nitrobenzyl)-4-methylpiperazine

https://huagongshe.com/reaction/883571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1-MethylpiperazineHCID 53167—
Reactant3-Chloro-4-nitrobenzaldehydeHCID 3769779—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventTolueneHCID 1140—
Product1-(3-Chloro-4-nitrobenzyl)-4-methylpiperazineHCID 5753894471.2%

Reaction Steps

N-methyl piperazine (2.50 mL, 22.5 mmol) was added dropwise to a solution of 3-chloro-4-nitrobenzaldehyde (2.09 g, 11.3 mmol) and acetic acid (0.29 mL, 5.14 mmol) in toluene (11.7 mL) at room temperature. The reaction mixture was stirred for 1.5 h at room temperature before the addition of further toluene (4.4 mL) and sodium triacetoxyborohydride (3.58 g, 16.9 mmol). The reaction mixture was stirred at room temperature overnight and then quenched by the addition of MeOH (3 mL) and saturated aqueous NaHCO3 (23 mL). The reaction mixture was stirred for 30 min. The phases were separated and the aqueous layer was extracted with toluene (2×30 mL). The combined organic extracts were concentrated under reduced pressure and purified by flash column chromatography (EtOAc:MeOH:NEt3 9:1:0.1) to give the title compound (2.17 g, 71%) as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08236954B2
Source datasetuspto-grants-2012_08
ORD IDord-fa22004cb70549f4aaf780cadbcd0b24
Source noteuspto-grants-2012_08