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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907832Generated: October 25, 2026

Sodium Iodide → 1-{4-[4-(3,4-Dichlorophenyl)piperazin-1-yl]butyl}-1,5,6,7-tetrahydroindol-4-one

https://huagongshe.com/reaction/1907832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(3,4-Dichlorophenyl)piperazineHCID 93601—
Reactant1-(4-Chlorobutyl)-1,5,6,7-tetrahydroindol-4-oneHCID 23502889—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
SolventDichloromethane ethylacetateHCID 21226138—
Product1-{4-[4-(3,4-Dichlorophenyl)piperazin-1-yl]butyl}-1,5,6,7-tetrahydroindol-4-oneHCID 1143007691.8%

Reaction Steps

A mixture of 1-(4-Chlorobutyl)-1,5,6,7-tetrahydroindol-4-one (600 mg) from step 1 and sodium iodide (438 mg) in acetonitrile (10 mL) was heated at reflux for 6 hours. (3,4-Dichlorophenyl)piperazine (581 mg) and potassium carbonate (367 mg) 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 (50 mL) and stirred for 0.5 hours. An oil separated out and was isolated from the mixture. The oil was dissolved with dichloromethane (15 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 (970 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598180B2
Source datasetuspto-grants-2013_12
ORD IDord-ee8769be30a24368a10e93b35b79195f
Source noteuspto-grants-2013_12