HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420835Generated: October 27, 2026
3,4-Dibromothiophene → 3,4-Bis(trimethylsilylethynyl)thiophene
https://huagongshe.com/reaction/420835
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,4-Dibromothiophene | HCID 18452 | — |
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | THF diisopropylamine | HCID 18968793 | — |
| Catalyst | Triphenylphosphine | HCID 11776 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Product | 3,4-Bis(trimethylsilylethynyl)thiophene | HCID 57681648 | — |
Reaction Steps
2.5 ml (22.6 mmol) of 3,4-dibromothiophene, commercially available from Aldrich under the Product No. 24,715-4, and 8 ml (56.5 mmol) of trimethylsilylacetylene were mixed with a solvent of tetrahydrofuran/diisopropylamine (1:1), and 0.15 g (0.23 mmol) of palladium dichlorodiphosphine, 21 mg (0.11 mmol) of copper iodide and 0.1 g (0.36 mmol) of triphenylphosphine were then sequentially added thereto. The reaction solution was heated at 70° C. for 8 hours, and washed with an aqueous solution of ammonium chloride. The resulting organic layer was dried over magnesium sulfate, dried under reduced pressure, and purified using silica gel column chromatography, thus obtaining 1.5 g of 3,4-bis(trimethylsilylethynyl)thiophene (IIa).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08097694B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-d12e9b942f61492b9e1d970331ec83a6 |
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| Source note | uspto-grants-2012_01 |
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