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HRID 35283作成日:2026年10月24日

Benzyl Bromide → 5-(Benzyloxy)-2-methoxybenzaldehyde

https://huagongshe.com/ja/reaction/35283

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物Sodium HydroxideHCID 14798—
反応物5-Hydroxy-2-MethoxybenzaldehydeHCID 358341—
触媒Trioctylmethylammonium chlorideHCID 21218—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物5-(Benzyloxy)-2-methoxybenzaldehydeHCID 1096669491%

反応手順

To a stirred suspension of 5-hydroxy-2-methoxybenzaldehyde (306.6 g, prepared by the method of Ulrich et al, J.Org.Chem., 1974, 39, 2437), benzyl bromide (355.8 g) and Adogen 464 (48.5 g) in dichloromethane (600 ml) was added a solution of sodium hydroxide (123.5 g) in water (500 ml). The mixture became warm and the suspension dissolved; additional dichloromethane (300 ml) was added to prevent crystallisation of the benzylated product. After 2 hours, the organic layer was removed, washed twice with water, once with saturated sodium chloride solution, then dried with anhydrous magnesium sulphate. The solution was concentrated, then treated with petroleum spirit to give 5-benzyloxy-2-methoxybenzaldehyde (445.7 g, 91%), m.p. 99°-100°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04766121
出典データセットuspto-grants-1988_08
ORD IDord-09acaa2b0fe944e185cdd2596e974e13
出典メモuspto-grants-1988_08