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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340252Generated: October 30, 2026

Triethylamine → 5-[(Triethylsilyl)ethynyl]-1H-indole

https://huagongshe.com/reaction/340252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(Triethylsilyl)acetyleneHCID 637947—
Reactantiodo-1H-indoleHCID 21086119—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
Product5-[(Triethylsilyl)ethynyl]-1H-indoleHCID 66893233—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a scintillation vial was added -iodo-1H-indole (1.1 eq.), triethyl(ethynyl)silane (1 eq.), triethylamine (5 eq.), and anhydrous DMF (0.2 M). Vacuumed and nitrogen flushed for three times. CuI (0.1 eq.) and bis(triphenylphosphine)dichloro-palladium(II) (0.1 eq) were added. The vial was sealed and heated at 60° C. overnight. Upon completion of the reaction as monitored by TLC, the content of the vial was loaded onto a silica gel column pretreated with hexanes. Column was washed with hexanes and diethylether until all eluents containing product were collected. Carefully distill off hexanes and ether using rotary evaporator with minim heating afforded product 5-((triethylsilyl)ethynyl)-1H-indole as colorless oil, which was carried directly on to the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895577B2
Source datasetuspto-grants-2014_11
ORD IDord-c70f2e941fc54793b226a74c3d2e68c7
Source noteuspto-grants-2014_11