HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489147Generated: October 30, 2026
Hydrochloric Acid → 3-(3-Methoxyphenyl)indole
https://huagongshe.com/reaction/1489147
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Phenylhydrazine | HCID 7516 | — |
| Reactant | Methyl (3-methoxystyryl) ether | HCID 57248581 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-(3-Methoxyphenyl)indole | HCID 15428715 | — |
Reaction Steps
A 90 g portion of the abovementioned methyl (3-methoxystyryl) ether was dissolved in 100 ml of ethanol. Then the solution was added dropwise to a mixed solution of 59.3 g phenylhydrazine, 800 ml ethanol and 53 ml concentrated hydrochloric acid under reflux, and after the addition, reflux heating was continued for 2 more hours. The reaction mixture was then cooled to room temperature, and after adding water, sodium chloride and a small amount of ethyl acetate, the mixture was stirred and the precipitated crystals were collected by filtration. The crystals were dissolved in chloroform and washed with dilute hydrochloric acid and sodium bicarbonate aqueous solution. And the solution was dried and concentrated to obtain a residue. Then toluene was added to the residue, and after refluxed for one hour. After cooling, precipitated crystals were then collected by filtration to obtain 89.6 g of 3-(3-methoxyphenyl)indole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05677326 |
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| Source dataset | uspto-grants-1997_10 |
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| ORD ID | ord-a6500f2254a34099b8a941f7cb5e974f |
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| Source note | uspto-grants-1997_10 |
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