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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489147Generated: October 30, 2026

Hydrochloric Acid → 3-(3-Methoxyphenyl)indole

https://huagongshe.com/reaction/1489147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium ChlorideHCID 5234—
ReactantPhenylhydrazineHCID 7516—
ReactantMethyl (3-methoxystyryl) etherHCID 57248581—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product3-(3-Methoxyphenyl)indoleHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05677326
Source datasetuspto-grants-1997_10
ORD IDord-a6500f2254a34099b8a941f7cb5e974f
Source noteuspto-grants-1997_10