Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535834Generated: October 30, 2026

Water → 1-Methyl-4-(4-nitro-2-(trifluoromethyl)benzyl)piperazine

https://huagongshe.com/reaction/535834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant1-MethylpiperazineHCID 53167—
Reactant1-(Bromomethyl)-4-nitro-2-(trifluoromethyl)benzeneHCID 46838761—
SolventDichloromethaneHCID 6344—
Product1-Methyl-4-(4-nitro-2-(trifluoromethyl)benzyl)piperazineHCID 4683890667.4%

Reaction Steps

To a solution of crude 1-(bromomethyl)-2-(trifluoromethyl)-4-nitrobenzene (13.7 mmol, 60% pure) in CH2Cl2 (20 mL) was added Et3N (1.5 g, 15 mmol) and 4-methylpiperazine (1.5 g, 15 mmol). After stirring for 5 hrs at rt, 50 mL H2O was added, and the mixture was extracted with 50 mL CH2Cl2. The combined organic layer was dried over Na2SO4, filtered, concentrated, and the resulting residue was purified by silica gel chromatography (eluent: 10% MeOH in CH2Cl2) to give the product (67.4%, 2.8 g). 1H NMR (300 MHz, CDCl3) δ: 8.52 (1H, s), 8.37-8.40 (1H, d, J=9.0 Hz), 8.00-8.03 (1H, d, J=9.0 Hz), 3.85 (2H, s), 3.09-3.15 (2H, m), 2.90-2.93 (2H, m), 2.80-2.83 (2H, m), 2.67 (3H, s), 2.53-2.59 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859553B2
Source datasetuspto-grants-2014_10
ORD IDord-95b7bb4d13894ba886b37747d33ac322
Source noteuspto-grants-2014_10