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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198268Generated: November 2, 2026

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

https://huagongshe.com/reaction/1198268

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 residue 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 numberUS05280032
Source datasetuspto-grants-1994_01
ORD IDord-f133d42343194deaa8edcb2048fe623f
Source noteuspto-grants-1994_01