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HRID 275222作成日:2026年10月27日

4-Isopropoxybenzaldehyde → 1-Methoxy-2-(4-[isopropoxy]phenyl)ethene

https://huagongshe.com/reaction/275222

反応式

関与物質

役割名称HCID仕込み量
反応物4-IsopropoxybenzaldehydeHCID 250077—
反応物Sodium BicarbonateHCID 516892—
反応物Methoxymethyl-triphenylphosphonium chlorideHCID 2723798—
溶媒tert-Butyl methyl etherHCID 15413—
生成物1-Methoxy-2-(4-[isopropoxy]phenyl)etheneHCID 5405047893.7%

反応条件

温度0 °C

反応手順

A suspension of 140 g of methoxymethyl-triphenylphosphonium chloride in 400 ml of tert.-butyl methyl ether is treated with 45 g of potassium tert.-butylate within 5 minutes at 0° C. while gassing with nitrogen and the mixture is stirred for a further 10 minutes. Then, a solution of 41 g of 4-(isopropyloxy)-benzaldehyde in 100 ml of tert.-butyl methyl ether is added dropwise at 0° C. within 30 minutes. The reaction mixture is stirred at room temperature for a further 16 hours and then poured into 750 ml of 0.8N sodium hydrogen carbonate solution. The aqueous phase is separated and back-extracted with diethyl ether. The organic phase is washed neutral with water, dried over magnesium sulphate and concentrated. The residue is suspended in 800 ml of hexane. After cooling to 0° C. the triphenylphosphine oxide is filtered off and the filtrate is concentrated. Chromatography of the residue on silica gel with hexane/ethyl acetate (vol. 9:1) gives 45 g of pure 1-methoxy-2-(4-[isopropoxy]phenyl)ethene.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05393458
出典データセットuspto-grants-1995_02
ORD IDord-f7e197db34504310b76a939086711b95
出典メモuspto-grants-1995_02