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HRID 436006作成日:2026年10月25日

Sodium Hydroxide → 2-Ethyl-3-carboxy-benzo[b]thiophene

https://huagongshe.com/reaction/436006

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物BromineHCID 24408—
反応物2-Ethyl-3-acetyl-benzo[b]thiopheneHCID 21455088—
反応物Sodium BisulfiteHCID 23665763—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物2-Ethyl-3-carboxy-benzo[b]thiopheneHCID 2145508992%

反応条件

温度0 °C

反応手順

Into a one-litre flask equipped with a mechanical stirrer and a dropping-funnel were introduced 39 g (0.97 mol) of sodium hydroxide with 270 ml of water. The solution was cooled to 0° C by means of an ice-bath and 20 ml (0.333 mol) of bromine were then added through the dropping-funnel followed by 190 ml of dioxan, care being taken to maintain the temperature at 0° C. Finally, still at the same temperature, a solution of 22.6 g (0.111 mol) of 2-ethyl-3-acetyl-benzo[b]thiophene in 25 ml of dioxan were introduced drop-by-drop. The mixture was then allowed to return to room temperature and stirring was maintained for 2 hours. A solution of sodium bisulphite was then added and the reaction medium was acidified and extracted with ether. The organic phase was washed with water, dried and evaporated to dryness to give 20.2 g of 2-ethyl-3-carboxy-benzo[b]thiophene. Yield 92%; M.P. 136° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04007204
出典データセットuspto-grants-1977_02
ORD IDord-b31d435d497f4e3fbccbea2599042cdf
出典メモuspto-grants-1977_02