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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | 3,4-Bis(benzyloxy)benzaldehyde | HCID 79526 | — |
| 반응물 | 2-Amino-5-chloro-alpha-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol | HCID 54358865 | — |
| 반응물 | HCID 178511851 | HCID 178511851 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 2-(3,4-Dibenzyloxybenzyl)amino-5-chloro-alpha-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol | HCID 54423878 | 75.5% |
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
| 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-f1156755ca1643af932a9577860a226c |
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| 출처 메모 | uspto-grants-2002_03 |
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