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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 275879생성일: 2026년 10월 26일

Acetic Acid → 2-(2-Benzyloxybenzylamino)-5-chloro-alpha-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol

https://huagongshe.com/reaction/275879

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물2-(Benzyloxy)benzaldehydeHCID 344784—
반응물2-Amino-5-chloro-alpha-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcoholHCID 54358865—
반응물HCID 178511851HCID 178511851—
용매MethanolHCID 887—
생성물2-(2-Benzyloxybenzylamino)-5-chloro-alpha-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcoholHCID 54253509136.3%

반응 조건

온도60 °C

반응 단계

In methanol (20 ml) were dissolved 2-amino-5-chloro-α-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol (0.5 g) obtained in Example 1 (2) and 2-benzyloxybenzaldehyde (0.7 g). To the solution were added acetic acid (0.15 g) and cyano sodium borohydride (0.16 g). The mixture was stirred for 40 minutes at 60° C. The reaction mixture was concentrated, to which were added water (50 ml) and ethyl acetate (60 ml), followed by subjecting the mixture to extraction. The organic layer was separated, washed with water and dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was purified by means of a silica gel column chromatography to give 2-(2-benzyloxybenzylamino)-5-chloro-α-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol (1.05 g) as a colorless oily product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06352982B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-e03e120bc9604b8b8cbd75e46166267b
출처 메모uspto-grants-2002_03