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HRID 62834作成日:2026年10月23日

Benzyl Bromide → 4-(Benzyloxy)-3,5-difluorobenzaldehyde

https://huagongshe.com/ja/reaction/62834

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Cesium carbonateHCID 10796—
反応物3,5-Difluoro-4-hydroxybenzaldehydeHCID 10192584—
溶媒AcetonitrileHCID 6342—
生成物4-(Benzyloxy)-3,5-difluorobenzaldehydeHCID 1571402692%

反応手順

3,5-Difluoro-4-hydroxy-benzaldehyde obtained in Step A was dissolved in CH3CN (15 mL), and Cs2CO3(6.3 g, 19.23 mmol) was added to the solution. The mixture was cooled to 0˜5° C. Benzylbromide (1.1 mL, 9.23 mmol) was added slowly thereto, and the mixture was stirred at room temperature for 2 hours. After the termination of the reaction, the reactant was filtered and then concentrated under reduced pressure. The residue was purified by column chromatography (eluent, EtOAc/Hex=1/7) to obtain the title compound (1.76 g, 92%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09447044B2
出典データセットuspto-grants-2016_09
ORD IDord-a43a6fb9e8be42e3a3e74def7ffb4128
出典メモuspto-grants-2016_09