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HRID 344955作成日:2026年10月26日

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

https://huagongshe.com/reaction/344955

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 50 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): & 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US05053523
出典データセットuspto-grants-1991_10
ORD IDord-30663fca9e604c7e84237d25f5ba12a8
出典メモuspto-grants-1991_10