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HRID 881780作成日:2026年10月27日

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

https://huagongshe.com/reaction/881780

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物4,7-Dibromo-2,1,3-benzothiadiazoleHCID 626361—
反応物2-Thiopheneboronic acidHCID 2733960—
触媒HCID 178418397HCID 178418397—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物4,7-Di(thiophen-2-yl)benzo(c)(1,2,5)thiadiazoleHCID 396294—

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08993697B2
出典データセットuspto-grants-2015_03
ORD IDord-56a7ee08aeeb4f2fa1a7d2a991458e63
出典メモuspto-grants-2015_03