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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 976543Generated: October 29, 2026

Ethanol hydrochloride → 1-(1H-inden-6-yl)-2-[2-(N,N-dimethylamino)ethoxy]ethanol hydrochloride

https://huagongshe.com/reaction/976543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanol hydrochlorideHCID 21887872—
ReactantSodium methanolate methanolHCID 23694274—
Reactant1-acetoxy-1-(1H-inden-6-yl)-2-[2-(N,N-dimethylamino)ethoxy]ethaneHCID 54373030—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
Product1-(1H-inden-6-yl)-2-[2-(N,N-dimethylamino)ethoxy]ethanol hydrochlorideHCID 67595883—

Reaction Steps

In 0.5 ml of methanol was dissolved 80 mg of 1-acetoxy-1-(1H-inden-6-yl)-2-[2-(N,N-dimethylamino)ethoxy]ethane. To the solution was added 80 mg of a 28% sodium methoxide-methanol solution with ice cooling. The resulting mixture was stirred at room temperature for 20 minutes. The solvent was removed by distillation under reduced pressure. The reside thus obtained was purified by column chromatography (eluant: chloroform/methanol=20/1) to obtain a yellow oily product. The oily product was dissolved in 0.1 ml of ethanol. To the solution was added 0.1 ml of a 5.9N dry hydrogen chloride-ethanol solution at room temperature. The resulting crystals were collected by filtration to obtain 20 mg of 1-(1H-inden-6-yl)-2-[2-(N,N-dimethylamino)ethoxy]ethanol hydrochloride (compound No. 298).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05612381
Source datasetuspto-grants-1997_03
ORD IDord-ac9fa80449764651884fe875ddc339f8
Source noteuspto-grants-1997_03