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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(3-(Trifluoromethyl)phenyl)piperazine | HCID 4296 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Diacetone Alcohol | HCID 31256 | — |
| Reactant | 1-(4-Chlorobutyl)-1,5,6,7-tetrahydroindol-4-one | HCID 23502889 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Dichloromethane ethylacetate | HCID 21226138 | — |
| Product | 1-{4-[4-(3-Trifluoromethylphenyl)piperazin-1-yl]butyl}-1,5,6,7-tetrahydroindol-4-one | HCID 9931885 | 91.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06770638B2 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-4b8bca94ec634a4d8da77fa4b45188a1 |
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| Source note | uspto-grants-2004_08 |
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