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HRID 39291作成日:2026年10月23日

Triethylamine → 5-(3,3-Dimethyl-but-1-ynyl)-thiophene-2-carboxylic acid ethyl ester

https://huagongshe.com/ja/reaction/39291

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物3,3-Dimethyl-1-butyneHCID 13512—
反応物Ethyl 5-bromothiophene-2-carboxylateHCID 605723—
触媒Copper iodideHCID 83717—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒DimethylformamideHCID 6228—
生成物5-(3,3-Dimethyl-but-1-ynyl)-thiophene-2-carboxylic acid ethyl esterHCID 5811412897.3%

反応手順

A mixture of 5-Bromo-thiophene-2-carboxylic acid ethyl ester (7 g, 30 mmol), copper iodide (1.2 g, 6 mmol), triethylamine (20 mL) in DMF (100 mL) was degassed in a 350 mL pressure bottle. Then tris(dibenzylideneacetone)dipalladium(0) (2.1 g, 3 mmol) and 3,3-dimethyl-but-1-yne (18.3 mL, 150 mmol) were added and heated at 80 degree for 3 hours. The reaction mixture was filtered on celite and washed with ethyl acetate. The solution was diluted with water and extracted twice with ethyl acetate. The organic phases were combined and washed with water. After drying and concentration, the crude residue was purified by flash chromatography to yield 6.9 g (95%) of 5-(3,3-Dimethyl-but-1-ynyl)-thiophene-2-carboxylic acid ethyl ester as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524764B2
出典データセットuspto-grants-2013_09
ORD IDord-32d5be6c632a4182b5049936e8f684b9
出典メモuspto-grants-2013_09