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HRID 1888843Erstellt: 27. Oktober 2026

Sodium Carbonate → 4,7-Di(thiophen-2-yl)benzo(c)(1,2,5)thiadiazole

https://huagongshe.com/reaction/1888843

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
Edukt4,7-Dibromo-2,1,3-benzothiadiazoleHCID 626361—
Edukt2-Thiopheneboronic acidHCID 2733960—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
Produkt4,7-Di(thiophen-2-yl)benzo(c)(1,2,5)thiadiazoleHCID 396294—

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08501889B2
Quelldatensatzuspto-grants-2013_08
ORD IDord-073591fbf5a74597a2a870f53db91317
Quellennotizuspto-grants-2013_08