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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

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물4-BenzyloxyphenylacetaldehydeHCID 11413489—
반응물2-Amino-5-chloro-alpha-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcoholHCID 54358865—
반응물HCID 178511852HCID 178511852—
용매MethanolHCID 887—
용매Ethyl AcetateHCID 8857—
생성물2-[2-(4-Benzyloxyphenyl)ethyl]amino-alpha-(3-tert-butoxycarbonylaminomethylphenyl)-5-chloro-benzyl alcoholHCID 54258279—

반응 조건

온도60 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06352982B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-1c8c5b7df28743a49d051f48e5d4a748
출처 메모uspto-grants-2002_03