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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | 2-(Benzyloxy)benzaldehyde | HCID 344784 | — |
| 반응물 | 2-Amino-5-chloro-alpha-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol | HCID 54358865 | — |
| 반응물 | HCID 178511851 | HCID 178511851 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 2-(2-Benzyloxybenzylamino)-5-chloro-alpha-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol | HCID 54253509 | 136.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US06352982B1 |
|---|
| 출처 데이터셋 | uspto-grants-2002_03 |
|---|
| ORD ID | ord-e03e120bc9604b8b8cbd75e46166267b |
|---|
| 출처 메모 | uspto-grants-2002_03 |
|---|