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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-DibromothiopheneHCID 18452—
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantTHF diisopropylamineHCID 18968793—
CatalystTriphenylphosphineHCID 11776—
CatalystCopper iodideHCID 83717—
Product3,4-Bis(trimethylsilylethynyl)thiopheneHCID 57681648—

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08097694B2
Source datasetuspto-grants-2012_01
ORD IDord-d12e9b942f61492b9e1d970331ec83a6
Source noteuspto-grants-2012_01