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HRID 5894作成日:2026年10月24日

Benzyl Bromide → 2-(Benzyloxy)-3-methoxybenzaldehyde

https://huagongshe.com/ja/reaction/5894

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o-VanillinHCID 8991—
反応物Potassium CarbonateHCID 11430—
溶媒EthanolHCID 702—
生成物2-(Benzyloxy)-3-methoxybenzaldehydeHCID 126808793%

反応手順

A mixture of 196.0 g (1.30 mole) of o-vanillin (Aldrich), 200 g of benzyl bromide (Aldrich), 500 g of anhydrous potassium carbonate and 1,500 mL of absolute ethanol is heated, with stirring, at reflux for 6 hours. After cooling, the supernatant is decanted and the remainder is filtered. The combined filtrate and supernatant is concentrated at reduced pressure to remove solvent. The remaining oil is extracted into 1 L of ether. The ether solution is washed with 500 mL of water, 600 mL of 1% potassium hydroxide solution, and 500 mL of water and then dried (potassium carbonate) and concentrated to give 263.4 g (84% yield) of product; mp 41°-43° C. Reported mp, 43° C. (Chem. Abstr. 62:16110a).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05246943
出典データセットuspto-grants-1993_09
ORD IDord-0b20c9191db0436d9a89e14bbc14aaef
出典メモuspto-grants-1993_09