戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 359356作成日:2026年10月27日

3,4,5-Trimethoxybenzaldehyde → 2,2-Dimethyl-5-[2-(3,4,5-trimethoxyphenyl)ethenyl]-3(2H)-furanone

https://huagongshe.com/reaction/359356

反応式

関与物質

役割名称HCID仕込み量
反応物3,4,5-TrimethoxybenzaldehydeHCID 6858—
反応物Sodium HydroxideHCID 14798—
反応物3(2H)-Furanone, 2,2,5-trimethyl-HCID 137080—
溶媒EthanolHCID 702—
生成物2,2-Dimethyl-5-[2-(3,4,5-trimethoxyphenyl)ethenyl]-3(2H)-furanoneHCID 5371610683%

反応手順

To a mixture of 2,2,5-trimethyl-3(2H)-furanone (2.5 g, 19.8 mM) and 3,4,5-trimethoxybenzaldehyde (4.7 g, 23.8 mM) in ethanol was added 1N aqueous sodium hydroxide (4 mL, 4mM). After the reaction mixture was stirred for 48 hours at room temperature, the solution was concentrated to 50 mL and diluted with water (300 mL). The aqueous layer was extracted with diethyl ether (4×100 mL). The combined ethereal extracts were washed with saturated aqueous sodium chloride (50 mL), dried over magnesium sulfate, filtered and concentrated under reduced pressure to afford a dark yellow crystalline solid. The crude product was purified by chromatography (silica gel, petroleum ether-ethyl acetate) to give light yellow crystals (5.0 g, 83% yield), m.p. 149°-150° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05001126
出典データセットuspto-grants-1991_03
ORD IDord-35d8c43986d044b590463d0e55aa15d7
出典メモuspto-grants-1991_03