HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 242765Erstellt: 23. Oktober 2026
Sodium Hydroxide → 4,8-Bis(octyloxy)benzo[1,2-b:4,5-b']dithiophene
https://huagongshe.com/de/reaction/242765
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | (Benzo(1,2-b:4,5-b)dithiophene-4,8-dione) | HCID 288478 | — |
| Edukt | n-Octyl p-Toluenesulfonate | HCID 599296 | — |
| Katalysator | Zinc | HCID 23994 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 4,8-Bis(octyloxy)benzo[1,2-b:4,5-b']dithiophene | HCID 58280899 | 62% |
Reaktionsschritte
1.0 g (4.5 mmol) of benzo[1,2-b:4,5-b′]dithiophene-4,8-dione was mixed with 0.65 g (10 mmol) of zinc dust in a flask. Then, 4 ml of ethanol and 15 ml of 20% NaOH was added and the mixture was refluxed for 1 h. 4.3 mL octyl p-toluenesulfonate was added in portions with stirring until the color changed to red. The resulting precipitate was filtered, the filtrate was diluted with 100 mL water and extracted with 100 mL chloroform. The organic extraction was dried with anhydrous sodium sulfate and evaporated in vacuo. Column chromatography on silica gel using dichloromethane and hexanes mixed solvents yielded the pure title compound as a white solid (1.24 g, 62%). 1HNMR (CDCl3): δ0.88-0.91 (6H, t, J=7 Hz), 1.31-1.38 (16H, m), 1.54-1.58 (4H, m), 1.84-1.89 (4H, m), 4.26-4.29 (4H, J=7 Hz), 7.36-7.37 (2H, d, J=6 Hz), 7.47-7.48 (2H, d, J=6 Hz).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08653228B2 |
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| Quelldatensatz | uspto-grants-2014_02 |
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| ORD ID | ord-e6513fd96e714cfd9160974fededf51d |
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| Quellennotiz | uspto-grants-2014_02 |
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