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HRID 2361155作成日:2026年10月26日

Benzyl Bromide → 4-(Benzyloxy)-2-hydroxy-3-methylbenzaldehyde

https://huagongshe.com/reaction/2361155

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1,4-DioxaneHCID 31275—
反応物2,4-Dihydroxy-3-methylbenzaldehydeHCID 80395—
反応物Sodium BicarbonateHCID 516892—
溶媒WaterHCID 962—
生成物4-(Benzyloxy)-2-hydroxy-3-methylbenzaldehydeHCID 59761690—

反応条件

温度60 °C

反応手順

A mixture of 2,4-dihydroxy-3-methyl-benzaldehyde (3.31 g, 21.8 mmol), benzylbromide (4.09 g, 23.9 mmol), NaHCO3 (5.49 g, 65.4 mmol), 1,4-dioxane (30 mL) and water (12 mL) was stirred at 60° C. for overnight. Then the reaction mixture was cooled to RT, water (100 mL) was added, extracted with EtOAc (2×200 mL). The extract was dried over Na2SO4, evaporated. The residue was purified on SiO2 (25 g) column, hexane-EtOAc (0 to 5%). Yield 1.57 g (6.48 mmol, 29%) as off-white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08686005B2
出典データセットuspto-grants-2014_04
ORD IDord-392855616cfa4a6780a51f366183d291
出典メモuspto-grants-2014_04