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HRID 6556作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物TrimethylsilylacetyleneHCID 66111—
反応物6-Bromo-1,2,3,4-tetrahydro-4,4-dimethylquinolineHCID 10823932—
触媒Dichlorobis(triphenylphosphine)palladiumHCID 6102075—
溶媒TriethylamineHCID 8471—
生成物4,4-Dimethyl-6-trimethylsilylethynyl-1,2,3,4-tetrahydroquinolineHCID 15661134—

反応条件

温度50 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05248777
出典データセットuspto-grants-1993_09
ORD IDord-093606782439496bbfe40e499def95b8
出典メモuspto-grants-1993_09