HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888843Generated: October 26, 2026
Sodium Carbonate → 4,7-Di(thiophen-2-yl)benzo(c)(1,2,5)thiadiazole
https://huagongshe.com/reaction/1888843
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4,7-Dibromo-2,1,3-benzothiadiazole | HCID 626361 | — |
| Reactant | 2-Thiopheneboronic acid | HCID 2733960 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 4,7-Di(thiophen-2-yl)benzo(c)(1,2,5)thiadiazole | HCID 396294 | — |
Reaction Steps
A solution of 4,7-dibromobenzo[c][1,2,5]thiadiazole (3.0 g, 10.2 mmol) and thiophen-2-ylboronic acid (2.87 g, 22.4 mmol) in 150 mL of 1,2-dimethoxyethane and 50 mL anhydrous ethanol was carefully degassed by bubbling nitrogen through the solution. Next, 7.16 g (67.2 mmol) of sodium carbonate dissolved in 30 mL water was added. The resulting emulsion was degassed, and the catalyst Pd(PPh3)4 (200 mg, 0.17 mmol) was added. Afterwards, the mixture was refluxed under nitrogen overnight. After removal of the organic solvent by reduced pressure, the mixture was poured into water (300 mL) and was extracted with chloroform (3×40 mL). The organic phase was washed with water (30 mL), dried over magnesium sulphate, and the solvent was removed in vacuo. Purification by flash silica gel column chromatography [hexane:chloroform=1:1 (v/v)] followed by recrystallization from hexane/dichloromethane (DCM) yielded orange crystals of TBT (2.6 g, 84.9%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501889B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-073591fbf5a74597a2a870f53db91317 |
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| Source note | uspto-grants-2013_08 |
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