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HRID 1892600作成日:2026年10月25日

Diisopropylamine → Methyl 2-((trimethylsilyl)ethynyl)isonicotinate

https://huagongshe.com/reaction/1892600

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylamineHCID 7912—
反応物TrimethylsilylacetyleneHCID 66111—
反応物2-Bromo-isonicotinic acid methyl esterHCID 3847768—
触媒Copper iodideHCID 83717—
触媒HCID 178418476HCID 178418476—
溶媒AcetonitrileHCID 6342—
生成物Methyl 2-((trimethylsilyl)ethynyl)isonicotinateHCID 6715119082%

反応条件

温度10 °C

反応手順

Methyl 2-bromoisonicotinate (216 g, 1 mol), dry acetonitrile (1.7 L), ethynyl(trimethyl)silane (117 g, 1.2 mol), diisopropylamine (122 g, 1.2 mol), and dichlorobis(triphenylphosphine)palladium (36 g, 0.05 mol) were placed into a well dried three necked flask which was twice purged with a stream of nitrogen. The reaction mixture was stirred for 0.5 hours, cooled to 10° C. and copper iodide (19 g, 0.1 mol) was added under a stream of nitrogen. At 20° C., the reaction mixture became thick and black and an exotherm was observed which was followed by formation of a precipitate. After the addition of copper iodide, the reaction mixture was stirred for further 2 hours at ambient temperature. The precipitated residue was separated by filtration and twice washed with diethyl ether (800 mL). The filtrate was washed with saturated ammonium chloride (2×300 mL) and brine (2×300 mL). After drying over sodium sulfate, the solvent was evaporated. The residue was purified using a silica gel column, eluting with hexane followed by 5% ethyl acetate in petroleum ether to yield 191 g (82%) of methyl 2-((trimethylsilyl)ethynyl)isonicotinate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08507681B2
出典データセットuspto-grants-2013_08
ORD IDord-bef50e358f674e54988b4cefd01ce4ef
出典メモuspto-grants-2013_08