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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,5-dibromo-3,4-dimethylthieno[2,3-b]thiophene | HCID 2820162 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 178442413 | HCID 178442413 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 23070268 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07183418B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-cc216c3dd21040b7992e4494986f7e52 |
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| Source note | uspto-grants-2007_02 |
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