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HRID 1521作成日:2026年10月23日

Methyl 5-(benzyloxy)-2-hydroxybenzoate → 4-(Benzyloxy)-2-(hydroxymethyl)phenol

https://huagongshe.com/ja/reaction/1521

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 5-(benzyloxy)-2-hydroxybenzoateHCID 13026913—
反応物Aluminium lithium hydrideHCID 21226445—
溶媒TetrahydrofuranHCID 8028—
生成物4-(Benzyloxy)-2-(hydroxymethyl)phenolHCID 19690921—

反応条件

温度0 °C

反応手順

Lithium aluminium hydride (0.235 g, 6.2 mMol) was suspended in tetrahydrofuran (25 ml) and cooled to 0° C. 5-Benzyloxy-2-hydroxy benzoic acid methyl ester (2 g, 7.75 mMol) in tetrahydrofuran (10 ml) was added dropwise, via cannula. The mixture was warmed to room temperature and stirred for 20 minutes. The reaction was then cooled to 0° C. and cautiously quenched by the addition of water (0.5 ml), 2M sodium hydroxide solution (0.5 ml), and water (1 ml). The resulting mixture was stirred at room temperature for 30 minutes and filtered. The filtrate was evaporated in vacuo to yield 4-benzyloxy-2-hydroxymethyl phenol as a clear oil which was used in the next step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05726165
出典データセットuspto-grants-1998_03
ORD IDord-d01bdcbca7ae4670b375df3584280165
出典メモuspto-grants-1998_03