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HRID 725608作成日:2026年10月25日

Sodium hydride → 4-(Benzyloxy)-3-(3-methoxypropoxy)benzaldehyde

https://huagongshe.com/reaction/725608

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物1-Bromo-3-methoxypropaneHCID 524551—
反応物4-Benzyloxy-3-hydroxybenzaldehydeHCID 561369—
溶媒DimethylformamideHCID 6228—
生成物4-(Benzyloxy)-3-(3-methoxypropoxy)benzaldehydeHCID 21458608—

反応手順

A solution of 28.8 g of 4-benzyloxy-3-hydroxy-benzaldehyde in 100 ml of dimethylformamide is added dropwise to a suspension of 5.54 g of NaH (60% dispersion in mineral oil) in 150 ml of absolute dimethylformamide. The reaction mixture is stirred at room temperature. After 30 minutes, a solution of 29 g of 3-methoxybromopropane in 120 ml of dimethylformamide is added thereto, and the mixture is stirred at room temperature for a further 4 hours and is then concentrated by evaporation under reduced pressure. The residue is partitioned between diethyl ether and water. The combined organic phases are dried over sodium sulfate and concentrated by evaporation, and the residue is purified by FC (100 g of silica gel, dichloromethane), yielding the title compound, which crystallises spontaneously: Rf (dichloromethane/diethyl ether)=0.44.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05705658
出典データセットuspto-grants-1998_01
ORD IDord-faf4937201404705974201b8e408253e
出典メモuspto-grants-1998_01