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HRID 68614作成日:2026年10月24日

3-Bromo-4-hydroxybenzaldehyde → 3-Bromo-4-((4-methoxybenzyl)oxy)benzaldehyde

https://huagongshe.com/ja/reaction/68614

反応式

関与物質

役割名称HCID仕込み量
反応物3-Bromo-4-hydroxybenzaldehydeHCID 76308—
反応物DiisopropylethylamineHCID 81531—
反応物4-Methoxybenzyl bromideHCID 165021—
溶媒DichloromethaneHCID 6344—
生成物3-Bromo-4-((4-methoxybenzyl)oxy)benzaldehydeHCID 23010223100%

反応手順

To a solution of 3-bromo-4-hydroxybenzaldehyde (5.0 g, 24.9 mmol; 1 eq) in DCM (10 mL), was added 1-(bromomethyl)-4-methoxybenzene (6.0 g, 29.88 mmol, 1.2 eq, Aldrich, Milwaukee, Wis., USA) and DIEA (8.7 mL, 49.7 mmol, 2 eq). After stirring at room temperature for 18 h, the reaction mixture was diluted with DCM and washed with saturated NaHCO3 and brine. The organic layer was dried (Na2SO4), filtered and concentrated in vacuo to give 8.0 g of 4-(4-methoxybenzyloxy)-3-bromobenzaldehyde (32).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822467B2
出典データセットuspto-grants-2014_09
ORD IDord-095c940df06246f88c3e22d39134361a
出典メモuspto-grants-2014_09