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HRID 2211742作成日:2026年10月25日

Water → N-[4-[[(E)-3-(4-Isopropylphenyl)-2-propenyl]oxy]-2,3,6-trimethylphenyl]formamide

https://huagongshe.com/reaction/2211742

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium hydrideHCID 24758—
反応物N-(4-hydroxy-2,3,6-trimethylphenyl)formamideHCID 21961295—
反応物1-[(E)-3-bromo-1-propenyl]-4-isopropylbenzeneHCID 21961313—
溶媒DimethylformamideHCID 6228—
生成物N-[4-[[(E)-3-(4-Isopropylphenyl)-2-propenyl]oxy]-2,3,6-trimethylphenyl]formamideHCID 2196134259.3%

反応手順

To a solution of N-(4-hydroxy-2,3,6-trimethylphenyl)formamide (5.20 g, 29.0 mmol) in N,N-dimethylformamide (30 ml) was added at 0° C. under a nitrogen atmosphere sodium hydride (a 60% dispersion in liquid paraffin, 1.39 g, 34.8 mmol) and the resulting mixture was stirred at the same temperature for 10 minutes. To the reaction solution was added 1-[(E)-3-bromo-1-propenyl]-4-isopropylbenzene (9.00 g, 37.7 mmol) and the resulting mixture was stirred at room temperature for 30 minutes. Water was added into the reaction solution and the product was extracted twice with ethyl acetate. The combined extracts were washed with water, dried on magnesium sulfate, and then concentrated under reduced pressure. The resulting residue was crystallized from ethyl acetate-hexane to obtain 5.80 g (59% yield) of the title compound. Melting point: 165-167° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07101867B2
出典データセットuspto-grants-2006_09
ORD IDord-ef768ddfeb8d47bfb0c9e57e5709577e
出典メモuspto-grants-2006_09