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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3-(4-Methoxy-phenoxy)-propylamine | HCID 3152109 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | n-butyl (R)-2-(3-formylphenoxy)butyrate | HCID 11846216 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | butyl (R)-2-(3-(((3-(4-methoxyphenoxy)propyl)amino)methyl)phenoxy)butanoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07538242B2 |
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| 출처 데이터셋 | uspto-grants-2009_05 |
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| ORD ID | ord-327652398a9a490d921bd1883f59e10a |
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| 출처 메모 | uspto-grants-2009_05 |
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