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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 250195생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/250195

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물5-MethoxybenzofuranHCID 25943—
반응물HCID 58088435HCID 58088435—
용매MethanolHCID 887—
생성물[3-(5-Methoxy-benzofuran-2-yl)-3-phenyl-propyl]-methyl-amineHCID 11623507—

반응 조건

온도110 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07863305B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-8bfd3924d9a14e69914d03f9d7cc7dba
출처 메모uspto-grants-2011_01