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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340253Generated: October 29, 2026

Tetrabutylammonium Fluoride → 5-Ethynyl-1H-indole

https://huagongshe.com/reaction/340253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant5-[(Triethylsilyl)ethynyl]-1H-indoleHCID 66893233—
SolventTetrahydrofuranHCID 8028—
Product5-Ethynyl-1H-indoleHCID 17842585—

Reaction Steps

To a stirred solution of 5-((triethylsilyl)ethynyl)-1H-indole (from the previous step) in THF (0.2 M) cooled at 0° C. was treated with a solution (0.5 eq.) of tetrabutylammonium fluoride in a dropwise fashion. The reaction mixture turned black and was continued to stir for 30 minutes before warming up to rt. TLC showed full conversion. The reaction was quenched with water and was extracted with diethylether. Combined organic layers were dried over anhydrous Na2SO4 and concentrated using rotary evaporator with minim heating. Chromatography (silica gel, diethylether) afforded the product 5-ethynyl-1H-indole as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895577B2
Source datasetuspto-grants-2014_11
ORD IDord-9e541765ed964fadaf928b3a44be6293
Source noteuspto-grants-2014_11