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HRID 77950作成日:2026年10月23日

3-Hydroxybenzaldehyde → 3-Benzyloxybenzaldehyde

https://huagongshe.com/ja/reaction/77950

反応式

関与物質

役割名称HCID仕込み量
反応物3-HydroxybenzaldehydeHCID 101—
反応物Benzyl BromideHCID 7498—
反応物Potassium CarbonateHCID 11430—
溶媒DimethylformamideHCID 6228—
生成物3-BenzyloxybenzaldehydeHCID 7434299%

反応手順

3-Hydroxybenzaldehyde (3 g, 24.6 mmol) and potassium carbonate (10.2 g, 73.8 mmol) were suspended in N,N-dimethylformamide (60 mL). Benzyl bromide (3.21 mL, 27.1 mmol) was added to this suspension, and stirred for 14 hours at room temperature. This mixture was partitioned into ethyl acetate and water. The organic layer was separated, washed with water, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure, and the residue was purified by silica gel column chromatography (heptane:ethyl acetate=4:1-1:1) to obtain the title compound (5.16 g, 99%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841327B2
出典データセットuspto-grants-2014_09
ORD IDord-daf2bdcd1dad47bc8ce5a045df540372
出典メモuspto-grants-2014_09