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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835087Generated: October 26, 2026

1-(3-(Trifluoromethyl)phenyl)piperazine → 1-{4-[4-(3-Trifluoromethylphenyl)piperazin-1-yl]butyl}-1,5,6,7-tetrahydroindol-4-one

https://huagongshe.com/reaction/1835087

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-(Trifluoromethyl)phenyl)piperazineHCID 4296—
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
ReactantDiacetone AlcoholHCID 31256—
Reactant1-(4-Chlorobutyl)-1,5,6,7-tetrahydroindol-4-oneHCID 23502889—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
SolventDichloromethane ethylacetateHCID 21226138—
Product1-{4-[4-(3-Trifluoromethylphenyl)piperazin-1-yl]butyl}-1,5,6,7-tetrahydroindol-4-oneHCID 993188591.5%

Reaction Steps

A mixture of 1-(4-Chlorobutyl)-1,5,6,7-tetrahydroindol-4-one (6.0 g, 26.6 mmol, as a mixture with 3.0 g of 4-hydroxy-4-methyl-2-pentanone) and sodium iodide (4.38 g, 29.2 mmol) in acetonitrile (100 mL) was heated at reflux for 6 h. (3-Trifluoromethylphenyl)piperazine (5.81 g, 25.2 mmol) and potassium carbonate (3.67 g, 26.6 mmol) was then added and reflux continued for 16 h. TLC (ethyl acetate:dichloromethane 1:1) showed complete reaction. The reaction was poured into ice cold water (400 mL) and stirred for 0.5 h. An oil separated out and was isolated from the mixture. The oil was dissolved with dichloromethane (150 mL), washed with water and brine, then dried with sodium sulfate, filtered and the solvent removed under vacuum to yield the title compound as an oil (9.7 g, 91.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06770638B2
Source datasetuspto-grants-2004_08
ORD IDord-4b8bca94ec634a4d8da77fa4b45188a1
Source noteuspto-grants-2004_08