HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340252Generated: October 30, 2026
Triethylamine → 5-[(Triethylsilyl)ethynyl]-1H-indole
https://huagongshe.com/reaction/340252
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (Triethylsilyl)acetylene | HCID 637947 | — |
| Reactant | iodo-1H-indole | HCID 21086119 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-[(Triethylsilyl)ethynyl]-1H-indole | HCID 66893233 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08895577B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-c70f2e941fc54793b226a74c3d2e68c7 |
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| Source note | uspto-grants-2014_11 |
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