Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12626Generated: October 26, 2026

Ethanol → ethyl 4-{1-[2-(ethyloxy)-2-oxoethyl]-7-ethynyl-1H-indol-3-yl}butanoate

https://huagongshe.com/reaction/12626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium CarbonateHCID 11430—
Reactantethyl 4-{1-[2-(ethyloxy)-2-oxoethyl]-7-[(trimethylsilyl)ethynyl]-1H-indol-3-yl}butanoateHCID 68692658—
SolventWaterHCID 962—
Productethyl 4-{1-[2-(ethyloxy)-2-oxoethyl]-7-ethynyl-1H-indol-3-yl}butanoateHCID 86622003—

Reaction Steps

To an ethanol (2 mL) solution of ethyl 4-{1-[2-(ethyloxy)-2-oxoethyl]-7-[(trimethylsilyl)ethynyl]-1H-indol-3-yl}butanoate (98 mg), potassium carbonate (50 mg) was added and the mixture was stirred at room temperature for 3 hours. To the reaction mixture, water was added, followed by extraction with ethyl acetate. The organic layer was washed with saturated saline, dried over anhydrous sodium sulfate and then concentrated to obtain the titled compound having the following physical properties (74 mg). Herein, ethyl 4-{1-[2-(ethyloxy)-2-oxoethyl]-7-[(trimethylsilyl)ethynyl]-1H-indol-3-yl}butanoate was prepared by the same operation as in Example 3, except for using ethyl 4-{7-bromo-1-[2-(ethyloxy)-2-oxoethyl]-1H-indol-3-yl}butanoate and ethynyl(trimethyl)silane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728023B2
Source datasetuspto-grants-2010_06
ORD IDord-84f48ebed0bb446fb2cd7436530f7815
Source noteuspto-grants-2010_06