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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-(2-Methoxyphenyl)piperazineHCID 1346—
ReactantIndole-3-CarbinolHCID 3712—
ReactantPotassium HydroxideHCID 14797—
ReactantLithium BromideHCID 82050—
ReactantTetrafluoro-m-phenylenediamine dihydrochlorideHCID 149026—
SolventEthanolHCID 702—
Product1H-Indole, 3-[[4-(2-methoxyphenyl)-1-piperazinyl]methyl]-HCID 281204559%

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05142052
Source datasetuspto-grants-1992_08
ORD IDord-68b9bf8db1914949b05a271879e5cc93
Source noteuspto-grants-1992_08