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HRID 6490作成日:2026年10月23日

Phenylacetylene → 1-(3,4,5-Trimethoxyphenyl)-3-phenyl-2-propyne-1-one

https://huagongshe.com/ja/reaction/6490

反応式

関与物質

役割名称HCID仕込み量
反応物PhenylacetyleneHCID 10821—
反応物N,3,4,5-tetramethoxy-N-methyl-BenzamideHCID 267535—
反応物Lithium bis(trimethylsilyl)amideHCID 57426343—
溶媒TetrahydrofuranHCID 8028—
生成物1-(3,4,5-Trimethoxyphenyl)-3-phenyl-2-propyne-1-oneHCID 1476338934.9%

反応手順

Place lithium hexamethyldisilazane (3 mL of a 1M solution in tetrahydrofuran, 3 mmol) and tetrahydrofuran (10 mL) under an argon atmosphere and cool to 0° C. Add phenylacetylene (0.33 mL, 3 mmol) and stir at 0° C. for 30 minutes. Add N-methoxy-N-methyl-(3,4,5-trimethoxy)benzamide (0.76 g, 3 mmol), remove the cooling bath and stir at room temperature for 1 hour. Partition between ethyl ether and saturated aqueous sodium chloride, separate the organic phase and dry (MgSO4). Filter and evaporate the solvent in vacuo. Pour onto silica gel and elute with 20% ethyl acetate/hexane to yield a crude solid. Recrystallize (hexane/ethyl acetate) to yield 0.31 g of the title compound; mp 94°-96° 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-49f779f24ab24cde9206b27accb4fa10
出典メモuspto-grants-1993_09