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HRID 1901342作成日:2026年10月27日

Sodium hydride → Ethyl 3-(5-bromobenzo[b]thien-2-yl)-2-ethoxycarbonyl-2-(4-methoxyphenyl)propionate

https://huagongshe.com/reaction/1901342

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物Ammonium ChlorideHCID 25517—
反応物Diethyl 2-(4-methoxyphenyl)malonateHCID 2785178—
反応物5-Bromo-2-(bromomethyl)benzo[b]thiopheneHCID 14819352—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 3-(5-bromobenzo[b]thien-2-yl)-2-ethoxycarbonyl-2-(4-methoxyphenyl)propionateHCID 2184420292.4%

反応手順

14.2 g of ethyl 2-ethoxycarbonyl-2-(4-methoxyphenyl)acetate was dissolved in 150 ml of tetrahydrofuran. 2.6 g of sodium hydride (oil type, 60%) was added to the above solution while stirring under ice cooling, and the stirring was continued for 20 minutes. To this was further added 17.2 g of 5-bromo-2-bromomethylbenzo[b]thiophene. After stirring at room temperature for 18 hours, the resulting reaction solution was mixed with ammonium chloride aqueous solution, and then extracted with ethyl acetate. After drying to distill off the solvent, the resulting residue was subjected to silica gel column chromatography using chloroform as an elution solvent, thereby obtaining 24.2 g of ethyl 3-(5-bromobenzo[b]thien-2-yl)-2-ethoxycarbonyl-2-(4-methoxyphenyl)propionate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05576343
出典データセットuspto-grants-1996_11
ORD IDord-cbf6f0c7b8de49e89b3363310600a5b5
出典メモuspto-grants-1996_11