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HRID 1004116作成日:2026年10月27日

4-Methoxyphenol → 5,6-Dimethoxy-3-(4-methoxyphenoxy)benzo[b]thiophene-2-carbaldehyde

https://huagongshe.com/reaction/1004116

反応式

関与物質

役割名称HCID仕込み量
反応物4-MethoxyphenolHCID 9015—
反応物Sodium hydrideHCID 24758—
反応物3-Chloro-5,6-dimethoxy-benzo[b]thiophene-2-carbaldehydeHCID 11780150—
溶媒DimethylformamideHCID 6228—
生成物5,6-Dimethoxy-3-(4-methoxyphenoxy)benzo[b]thiophene-2-carbaldehydeHCID 11089215—

反応手順

1.1 equivalents of sodium hydride and then 0.033 mol of the product obtained in Step D are added at room temperature and under an inert atmosphere to a solution of 0.036 mol of 4-methoxyphenol in 250 ml of dimethylformamide. After 12 hours' reaction, the reaction mixture is concentrated under reduced pressure. The residue is then diluted in ethyl acetate, washed with water and then with an aqueous NaCl solution, dried over calcium sulphate, filtered and concentrated under reduced pressure. Chromatography over silica gel (dichloromethane/ethyl acetate: 98/2) enables 8.6 g of the expected product to be isolated.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06048875
出典データセットuspto-grants-2000_04
ORD IDord-af71c7c070464d8989fd0df29414dfce
出典メモuspto-grants-2000_04