Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 275866생성일: 2026년 10월 25일
Acetic Acid → 2-[2-(4-Benzyloxyphenyl)ethyl]amino-alpha-(3-tert-butoxycarbonylaminomethylphenyl)-5-chloro-benzyl alcohol
https://huagongshe.com/reaction/275866
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | 4-Benzyloxyphenylacetaldehyde | HCID 11413489 | — |
| 반응물 | 2-Amino-5-chloro-alpha-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol | HCID 54358865 | — |
| 반응물 | HCID 178511852 | HCID 178511852 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 2-[2-(4-Benzyloxyphenyl)ethyl]amino-alpha-(3-tert-butoxycarbonylaminomethylphenyl)-5-chloro-benzyl alcohol | HCID 54258279 | — |
반응 단계
In methanol (15 ml) were dissolved 2-amino-5-chloro-α-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol produced in Example 1-(2) (0.5 g) and 4-benzyloxyphenylacetaldehyde (0.4 g). To the solution were added acetic acid (0.1 g) and, subsequently, cyano sodium hydride (0.11 g). The mixture was stirred for 40 minutes at 60° C. The reaction mixture was diluted with ethyl acetate (60 ml), which was washed with water and dried over anhydrous sodium sulfate. The solvent was distilled off to leave 2-[2-(4-benzyloxyphenyl)ethyl]amino-α-(3-tert-butoxycarbonylaminomethylphenyl)-5-chloro-benzyl alcohol (0.45 g) as a colorless oily product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06352982B1 |
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| 출처 데이터셋 | uspto-grants-2002_03 |
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| ORD ID | ord-1c8c5b7df28743a49d051f48e5d4a748 |
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| 출처 메모 | uspto-grants-2002_03 |
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