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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 881780Generated: October 26, 2026

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

https://huagongshe.com/reaction/881780

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4,7-Dibromo-2,1,3-benzothiadiazoleHCID 626361—
Reactant2-Thiopheneboronic acidHCID 2733960—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4,7-Di(thiophen-2-yl)benzo(c)(1,2,5)thiadiazoleHCID 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 degas sed, 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993697B2
Source datasetuspto-grants-2015_03
ORD IDord-56a7ee08aeeb4f2fa1a7d2a991458e63
Source noteuspto-grants-2015_03