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HRID 327753作成日:2026年10月26日

1-Propanol → 4-Ethenylphenyl-di-n-propoxymethane

https://huagongshe.com/reaction/327753

反応式

関与物質

役割名称HCID仕込み量
反応物1-PropanolHCID 1031—
反応物p-Toluenesulfonic acidHCID 6101—
反応物Sodium HydroxideHCID 14798—
反応物4-VinylbenzaldehydeHCID 39389—
溶媒BenzeneHCID 241—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
生成物4-Ethenylphenyl-di-n-propoxymethaneHCID 19733563—

反応手順

In a 100 ml 3-necked round-bottomed flask, 6.8 g (51.5 mmol) of 4-vinylbenzaldehyde, 12.4 g (205.8 mmol) of n-propanol and 0.1 g (0.5 mmol) of p-toluenesulfonic acid are dissolved in 45 ml of benzene. The solution is refluxed for 22 hours using a water separator and then ether is added thereto. The mixture is subsequently neutralised with 0.1N sodium hydroxide solution. The organic phase is then washed three times with water, dried over magnesium sulfate and concentrated. The resulting oil can be purified by column chromatography (stationary phase silica gel, mobile phase hexane/ether 5/4) to yield 2.54 g (10.8 mmol, 21% of the theoretical yield) of the desired substance in the form of a clear oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05274060
出典データセットuspto-grants-1993_12
ORD IDord-ae10a3d48b63427d8c466b82ddd5b310
出典メモuspto-grants-1993_12