HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847438Generated: October 30, 2026
Hydrochloric Acid → 1H-Indole, 3-[[4-(2-methoxyphenyl)-1-piperazinyl]methyl]-
https://huagongshe.com/reaction/847438
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-(2-Methoxyphenyl)piperazine | HCID 1346 | — |
| Reactant | Indole-3-Carbinol | HCID 3712 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Lithium Bromide | HCID 82050 | — |
| Reactant | Tetrafluoro-m-phenylenediamine dihydrochloride | HCID 149026 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1H-Indole, 3-[[4-(2-methoxyphenyl)-1-piperazinyl]methyl]- | HCID 2812045 | 59% |
Reaction Steps
One mole (147 g) of indole-3-carbinol and one mole (192 g) of 1-(2-methoxyphenyl)piperazine were dissolved in 1.5 liters of ethanol 60%. One mole (87 g) of lithium bromide and 0.1 mole (5.6 g) of potassium hydroxide were added, then the reaction medium was heated at reflux under stirring for 24 hours. After the reaction medium had cooled to 60° C., hydrochloric acid was added until persistence of an acidic pH. Then 189 g of the dihydrochloride salt of the title product was allowed to crystallize by cooling at 0° C. overnight, producing a global yield of 59% (m.p. 188°-190° C. with decomposition.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05142052 |
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| Source dataset | uspto-grants-1992_08 |
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| ORD ID | ord-68b9bf8db1914949b05a271879e5cc93 |
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| Source note | uspto-grants-1992_08 |
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