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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 495108생성일: 2026년 10월 25일

3-(4-Methoxy-phenoxy)-propylamine → butyl (R)-2-(3-(((3-(4-methoxyphenoxy)propyl)amino)methyl)phenoxy)butanoate

https://huagongshe.com/reaction/495108

반응식

참여 물질

역할이름HCID투입량
반응물3-(4-Methoxy-phenoxy)-propylamineHCID 3152109—
반응물Sodium borohydrideHCID 4311764—
반응물n-butyl (R)-2-(3-formylphenoxy)butyrateHCID 11846216—
용매MethanolHCID 887—
생성물butyl (R)-2-(3-(((3-(4-methoxyphenoxy)propyl)amino)methyl)phenoxy)butanoateHCID 57552765—

반응 단계

3-(4-Methoxyphenoxy)propylamine (34 mg) was dissolved in methanol (3 mL), and a solution (2 mL) of n-butyl (R)-2-(3-formylphenoxy)butyrate (50 mg) in methanol was added thereto under stirring at room temperature. The mixture was further stirred at 80° C. for 12 hours. Subsequently, an aqueous solution (0.5 mL) of sodium borohydride (7 mg) was added to the solution at room temperature, and the mixture was stirred for 30 minutes. The reaction solution was concentrated under reduced pressure, and chloroform was added to the concentrated product. The formed organic layer was washed with water. The washed organic layer was dried over sodium sulfate anhydrate, and concentrated under reduced pressure, to thereby yield 81 mg of a pale yellow, oily substance. The entirety of the substance was employed in the following reaction without any further treatment.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07538242B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-327652398a9a490d921bd1883f59e10a
출처 메모uspto-grants-2009_05