戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 75145作成日:2026年10月24日

4-Hydroxybenzaldehyde → Benzaldehyde, 4-(phenylmethoxy)-

https://huagongshe.com/ja/reaction/75145

反応式

関与物質

役割名称HCID仕込み量
反応物4-HydroxybenzaldehydeHCID 126—
反応物Potassium IodideHCID 4875—
反応物DimethylformamideHCID 6228—
反応物Potassium CarbonateHCID 11430—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物Benzaldehyde, 4-(phenylmethoxy)-HCID 7810995%

反応手順

To a stirred mixture of 4-hydroxybenzaldehyde (28.2 g, 231 mmol), potassium carbonate (47.9 g, 35 mmol), potassium iodide and DMF(280 mL) benzyl bromide was added slowly at 0° C. The mixture was stirred at rt overnight. The mixture was diluted with EtOAc and water. The layers were separated and the aqueous layer was extracted with EtOAc. The combined organic layers were washed with 1N aq HCl and dried. The solution was concentrated to give 4-benzyloxybenzaldehyde (46.5 g, 95%). 1H NMR: (CDCl3, 400 MHZ) δ=5.15 (s, 2H), 7.06 (m, 2H), 7.42(m, 5H), 7.84(m, 2H), 9.89(s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08835426B2
出典データセットuspto-grants-2014_09
ORD IDord-42ea015766b440f091058e5f05edbb7f
出典メモuspto-grants-2014_09