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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6556생성일: 2026년 10월 23일

Dichloromethane → 4,4-Dimethyl-6-trimethylsilylethynyl-1,2,3,4-tetrahydroquinoline

https://huagongshe.com/ko/reaction/6556

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물TrimethylsilylacetyleneHCID 66111—
반응물6-Bromo-1,2,3,4-tetrahydro-4,4-dimethylquinolineHCID 10823932—
촉매Dichlorobis(triphenylphosphine)palladiumHCID 6102075—
용매TriethylamineHCID 8471—
생성물4,4-Dimethyl-6-trimethylsilylethynyl-1,2,3,4-tetrahydroquinolineHCID 15661134—

반응 조건

온도50 °C

반응 단계

A solution of 1.608 g (6.7 mmol) of 4,4-dimethyl-6-bromo-1,2,3,4-tetrahydroquinoline (Compound 94) in 1.5 ml of triethylamine in a heavy-walled tube was degassed under argon and then treated with 75 mg (0.39 mmol) of cuprous iodide and 150 mg (0.21 mmol) of bis(triphenylphosphine) palladium (II) chloride. The mixture was degassed again under argon, treated with 2.09 g (21.2 mmol) of trimethylsilylacetylene and the tube was sealed. The mixture was heated at 50 degrees C. for 48 h. After cooling to room temperature methylene chloride was added to the reaction mixture and the mixture filtered. The filtrate was concentrated in vacuo and the residue purified by flash chromatography (silica; 10% ethyl acetate in hexanes) to give the title compound as a yellow oil. PMR (CDCl3): δ 0.20 (9H, s), 1.20 (6H, s), 1.57-1.63 (2H, m), 3.16-3.25 (2H, m), 4.02 (1H, broad s), 6.24 (1H, d, J~8.2 Hz), 7.00 (1H, dd, J~8.2 Hz, 1.8 Hz), 7.26 (1H, d, J~1.8 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05248777
출처 데이터셋uspto-grants-1993_09
ORD IDord-093606782439496bbfe40e499def95b8
출처 메모uspto-grants-1993_09