Zurück
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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
Edukt(Benzo(1,2-b:4,5-b)dithiophene-4,8-dione)HCID 288478—
Eduktn-Octyl p-ToluenesulfonateHCID 599296—
KatalysatorZincHCID 23994—
LösungsmittelEthanolHCID 702—
Produkt4,8-Bis(octyloxy)benzo[1,2-b:4,5-b']dithiopheneHCID 5828089962%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08653228B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-e6513fd96e714cfd9160974fededf51d
Quellennotizuspto-grants-2014_02