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HRID 250195作成日:2026年10月26日

Sodium Hydroxide → [3-(5-Methoxy-benzofuran-2-yl)-3-phenyl-propyl]-methyl-amine

https://huagongshe.com/reaction/250195

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5-MethoxybenzofuranHCID 25943—
反応物HCID 58088435HCID 58088435—
溶媒MethanolHCID 887—
生成物[3-(5-Methoxy-benzofuran-2-yl)-3-phenyl-propyl]-methyl-amineHCID 11623507—

反応条件

温度110 °C

反応手順

5-methoxybenzofuran (0.48 g) and trifluoro-acetic acid 3-[methyl-(2,2,2-trifluoro-acetyl)-amino]-1-phenyl-propyl ester (0.48 g) were mixed and heated in a sealed tube at 110° C. for 90 minutes. Upon cooling, the reaction mixture was taken up in methanol and treated with excess 1N sodium hydroxide solution, sufficient to form a strongly basic solution. After stirring for 20 minutes, the reaction mixture was concentrated at reduced pressure to remove the bulk of the methanol. The resulting mixture was partitioned between ethyl acetate and water. The layers were separated and the organic layer was evaporated to dryness. Purification by column chromatography (silica gel, dichloromethane (130):methanol (10):ammonium hydroxide (1)) followed by preparative tlc afforded [3-(5-Methoxy-benzofuran-2-yl)-3-phenyl-propyl]-methyl-amine (M+H=296) as the major component.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07863305B2
出典データセットuspto-grants-2011_01
ORD IDord-8bfd3924d9a14e69914d03f9d7cc7dba
出典メモuspto-grants-2011_01