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HRID 235404作成日:2026年10月23日

Acetovanillone → (Z)-1-[4-[(4-chloro-2-butenyl)oxy]-3-methoxyphenyl]ethanone

https://huagongshe.com/ja/reaction/235404

反応式

関与物質

役割名称HCID仕込み量
反応物AcetovanilloneHCID 2214—
反応物Potassium CarbonateHCID 11430—
反応物1,4-Dichloro-cis-2-buteneHCID 6432115—
溶媒AcetonitrileHCID 6342—
生成物(Z)-1-[4-[(4-chloro-2-butenyl)oxy]-3-methoxyphenyl]ethanoneHCID 57454977106.8%

反応手順

A stirred mixture of 4-hydroxy-3-methoxyacetophenone (16.6 g, 10 mmole), K2CO3 (14 g, 100 mmol) and cis-1,4-dichloro-2-butene (Aldrich, 15 g, 120 mmol) in acetonitrile (250 ml) was heated at reflux for 2.5 hours. The mixture was filtered and concentrated to an oil. Purification was by flash chromatography. The fractions containing the purest product were combined and concentrated to give white crystals, 7.7 g, 30%. This was recrystallized from ether to give analytical pure (Z)-1-[4-[(4-chloro-2-butenyl)oxy]-3-methoxyphenyl]ethanone (2.72 g), m.p.=64°-66° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05597842
出典データセットuspto-grants-1997_01
ORD IDord-b317ab15dd674038bd0fdf666fa472f9
出典メモuspto-grants-1997_01