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HRID 1443022作成日:2026年10月27日

Potassium Hydroxide → 2,5-Diethynylthiophene

https://huagongshe.com/reaction/1443022

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium HydroxideHCID 14797—
反応物TrimethylsilylacetyleneHCID 66111—
反応物2,5-DiiodothiopheneHCID 69368—
反応物2,5-Bis[(trimethylsilyl)ethynyl]thiopheneHCID 12702007—
触媒HCID 178418476HCID 178418476—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒TriethylamineHCID 8471—
生成物2,5-DiethynylthiopheneHCID 1134404072%

反応手順

To a 250 mL flask were added 2.5 g of 2,5-diiodothiophene (7.44 mmol), 100 mg of Cul, and 220 mg of Pd(Ph3P)2Cl2 under nitrogen. Then 100 mL of triethylamine (TEA) and 5.0 mL of trimethylsilylacetylene (3.40 g, 35 mmol) were injected. The reaction mixture was allowed to stir at room temperature for 12 hours. The precipitate was removed by filtration and the solvent of the filtrate was evaporated. The crude intermediate, i.e. 2,5-bis(trimethylsilylethynyl)thiophene, was purified by column chromatography and thus hydrolysed with 3 g KOH (53.6 mmol) in 70 mL methanol for 2 hours. The solution was poured into a large amount of water, and extracted with diethyl ether twice. The resultant solution was washed with water three times, dried over magnesium sulphate, and then the solvent was removed under reduced pressure to give 2,5-diethynylthiophene as a pale yellow liquid (0.71 g, 72%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07659353B2
出典データセットuspto-grants-2010_02
ORD IDord-5e5347f295cc447d854dddb9e4f2546a
出典メモuspto-grants-2010_02