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HRID 1757501作成日:2026年10月24日

N-Methoxy-N-methylbenzamide → 1-Phenyl-3-[3-(4-methoxybenzyloxy)phenyl]-2-propyne-1-one

https://huagongshe.com/ja/reaction/1757501

反応式

関与物質

役割名称HCID仕込み量
反応物N-Methoxy-N-methylbenzamideHCID 569575—
反応物1-Ethynyl-3-((4-methoxybenzyl)oxy)benzeneHCID 15281122—
反応物Lithium bis(trimethylsilyl)amideHCID 57426343—
溶媒TetrahydrofuranHCID 8028—
生成物1-Phenyl-3-[3-(4-methoxybenzyloxy)phenyl]-2-propyne-1-oneHCID 9840975—

反応条件

温度0 °C

反応手順

Place lithium hexamethyldisilazane (2 mL of a 1M solution in tetrahydrofuran, 2 mmol) and tetrahydrofuran (8 mL) under an argon atmosphere and cool to 0° C. Add a solution of 3-(4methoxybenzyloxy)phenylacetylene (0.48 g, 2 mmol) in tetrahydrofuran and stir the brown solution for 45 minutes at 0° C. Add N-methoxy-N-methylbenzamide (0.4 g, 2.4 mmol), remove the cooling bath andstir at room temperature for 1 hour. Partition the mixture between ethyl ether and water, separate the organic phase and dry (MgSO4). Filter and evaporate the solvent in vacuo to yield an oil. Filter through silica gel and elute with 10% ethyl acetate/hexane to yield a crude solid. Recrystallize (hexane, ethyl ether) to yield 0.26 g (lst crop) and 0.15 g (2nd crop) of the title compound; mp 79°-80 C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05446068
出典データセットuspto-grants-1995_08
ORD IDord-48780852258f42e2936b931423a3798e
出典メモuspto-grants-1995_08