戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 6492作成日:2026年10月23日

N-Methoxy-N-methylbenzamide → 1-Phenyl-3-(3-benzyloxyphenyl)-2-propyne-1-one

https://huagongshe.com/ja/reaction/6492

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-(Benzyloxy)-3-ethynylbenzeneHCID 19422228—
反応物Lithium bis(trimethylsilyl)amideHCID 57426343—
溶媒TetrahydrofuranHCID 8028—
生成物1-Phenyl-3-(3-benzyloxyphenyl)-2-propyne-1-oneHCID 1938821957%

反応条件

温度0 °C

反応手順

Place lithium hexamethyldisilazane (15 mL of a 1M solution in tetrahydrofuran, 15 mmol) and tetrahydrofuran (75 mL) under an argon atmosphere and cool with an ice-water bath. Add, by dropwise addition, a solution of 3-benzyloxyphenylacetylene (3.13 g, 15 mmol) in tetrahydrofuran. Stir at 0° C. for 45 minutes, then add, by dropwise addition, N-methoxy-N-methylbenzamide (2.45 mL, 16 mmol). Remove the cooling bath and stir at room temperature for 1 hour. Partition between ethyl ether and water, separate the organic phase and dry (MgSO4). Filter and evaporate the solvent in vacuo to yield a crude solid. Recrystallize (hexane/ethyl acetate) to yield 2.67 g (57%) of the title compound; mp 75°-77° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05248825
出典データセットuspto-grants-1993_09
ORD IDord-8b7ba583998740be987368a88e5eb0cd
出典メモuspto-grants-1993_09