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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428546Generated: October 26, 2026

(4-Amino-2-(trifluoromethyl)phenyl)(4-ethylpiperazin-1-yl)methanone → 4-((4-Ethylpiperazin-1-yl)methyl)-3-(trifluoromethyl)aniline

https://huagongshe.com/reaction/1428546

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Amino-2-(trifluoromethyl)phenyl)(4-ethylpiperazin-1-yl)methanoneHCID 90417522—
SolventTetrahydrofuranHCID 8028—
Product4-((4-Ethylpiperazin-1-yl)methyl)-3-(trifluoromethyl)anilineHCID 5913456469.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of (4-amino-2-trifluoromethyl-phenyl)-(4-ethyl-piperazin-1-yl)-methanone (20 g, 66.4 mmol) in THF (500 mL) was added BH3DMS (19.91 mL, 199 mmol) dropwise. Then the mixture was stirred at 80° C. for 4 h. The mixture was quenched by adding MeOH and then concentrated. The residue was purified by silica column chromatography on silica gel (PE:EA=2:1, Rf=0.35) to give a white solid of 4-(4-ethyl-piperazin-1-ylmethyl)-3-trifluoromethyl-phenylamine (14 g, 46.0 mmol, 69.4% yield): 1H NMR (400 MHz, CDCl3) δ: 7.48 (d, J=8.4 Hz, 1H), 6.91 (d, J=2.8 Hz, 1H), 6.79 (dd, J=2.4, 8.4 Hz, 1H), 3.76 (s, 2H), 3.53 (s, 2H), 2.45-2.39 (m, 8H), 1.08 (t, J=7.2 Hz, 3H); ES-LCMS m/z 288 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937071B2
Source datasetuspto-grants-2015_01
ORD IDord-2b82600c23eb4c9d9fe15a578eeedf97
Source noteuspto-grants-2015_01