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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 39291생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3,3-Dimethyl-1-butyneHCID 13512—
반응물Ethyl 5-bromothiophene-2-carboxylateHCID 605723—
촉매Copper iodideHCID 83717—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매DimethylformamideHCID 6228—
생성물5-(3,3-Dimethyl-but-1-ynyl)-thiophene-2-carboxylic acid ethyl esterHCID 5811412897.3%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524764B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-32d5be6c632a4182b5049936e8f684b9
출처 메모uspto-grants-2013_09