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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 275878생성일: 2026년 10월 26일

Acetic Acid → 2-(3,4-Dibenzyloxybenzyl)amino-5-chloro-alpha-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol

https://huagongshe.com/reaction/275878

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물3,4-Bis(benzyloxy)benzaldehydeHCID 79526—
반응물2-Amino-5-chloro-alpha-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcoholHCID 54358865—
반응물HCID 178511851HCID 178511851—
용매MethanolHCID 887—
생성물2-(3,4-Dibenzyloxybenzyl)amino-5-chloro-alpha-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcoholHCID 5442387875.5%

반응 조건

온도60 °C

반응 단계

In methanol (20 ml) were dissolved 2-amino-5-chloro-α-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol (0.6 g) and 3,4-dibenzyloxybenzaldehyde (0.55 g). To the solution were added acetic acid (0.12 g) and cyano sodium borohydride (0.13 g). The mixture was stirred for 1.5 hour at 60° C. The reaction mixture was concentrated, to which were added water (50 ml) and ethyl acetate (80 ml), followed by extraction. The organic layer was washed with water and dried over anhydrous sodium sulfate. The solvent was distilled off to leave 2-(3,4-dibenzyloxybenzyl)amino-5-chloro-α-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol (0.83 g) as colorless crystals, m.p.: 118-120° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06352982B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-f1156755ca1643af932a9577860a226c
출처 메모uspto-grants-2002_03