戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1717513作成日:2026年10月24日

Cesium carbonate → 5-Methoxy-2-(2-mesyloxyethoxy)-benzaldehyde

https://huagongshe.com/ja/reaction/1717513

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物1,2-Ethanediol, 1,2-dimethanesulfonateHCID 20796—
反応物2-Hydroxy-5-methoxybenzaldehydeHCID 95695—
溶媒DimethylformamideHCID 6228—
生成物5-Methoxy-2-(2-mesyloxyethoxy)-benzaldehydeHCID 5976585578%

反応条件

温度70 °C

反応手順

To a vigorously stirred solution of 15,2 g (100 mmol) 2-hydroxy-5-methoxy-benzaldehyde and 42.4 g (130 mmol) caesium carbonate in 350 ml DMF at 0° C. was added 27,3 g (125 mmol) 1,2-bis-methanesulfonyloxy-ethane ((J. Med. Chem.; 47; 17; (2004); 4300-4315) in 50 ml DMF dropwisely. The reaction mixture was stirred vigorously at 70° C. for 5 h. The solvent was evaporated. 200 ml water and 200 ml ethyl acetate were added. The organic phase was separated. The aqueous phase was extracted three times with 100 ml ethyl acetate each. The combined organic phases were washed with 50 ml water and 50 ml brine. The organic phase was dried with magnesium sulfate and evaporated. The crude product was purified by silica column chromatography (gradient ethylacetate:hexane 1:6, ethyl acetate→1:2). The desired product 4a was obtained in 78% yield (21.4 g, 78 mmol) as yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07803960B2
出典データセットuspto-grants-2010_09
ORD IDord-3d753c14c9994b67aa656b2412c7b636
出典メモuspto-grants-2010_09