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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351298Generated: October 30, 2026

2,5-dibromo-3,4-dimethylthieno[2,3-b]thiophene → HCID 23070268, compound

https://huagongshe.com/reaction/351298

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-dibromo-3,4-dimethylthieno[2,3-b]thiopheneHCID 2820162—
ReactantSodiumHCID 5360545—
ReactantHCID 178442413HCID 178442413—
SolventDiethyl EtherHCID 3283—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 23070268HCID 23070268—

Reaction Steps

To a solution of 2,5-dibromo-3,4-dimethylthieno[2,3-b]thiophene (3.02 g, 9.28 mmol) and sodium 4-hexylthiophene boronate (5.14 g, 20.4 mmol) in degassed DME (200 ml) was added tetrakis(triphenyl-phosphine)palladium(0) (0.5 g, 5 mol %). The solution was heated to reflux and a saturated solution of sodium hyodrogen carbonate (4.2 g, 49 mmol) was added slowly. The reaction was refluxed for 16 h, cooled and diluted with diethyl ether. The layers were separated and the organics washed with 5% HCl, brine, dried (Na2SO4), filtered and concentrated under reduced pressure. The crude product was purified by column chromatography over silica (eluent: petrol) to afford the product after recrystallisation from petroi (1.03 g, 22%). :M/Z 500 (M+). Found C, 66.9.1, H, 6.9, S, 25.3. Calc. for C28H36S4 C, 67.2; H 7.2, S, 25.6. NMR gave the expected signals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07183418B2
Source datasetuspto-grants-2007_02
ORD IDord-cc216c3dd21040b7992e4494986f7e52
Source noteuspto-grants-2007_02