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HRID 275878作成日:2026年10月27日
Acetic Acid → 2-(3,4-Dibenzyloxybenzyl)amino-5-chloro-alpha-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol
https://huagongshe.com/reaction/275878
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | 3,4-Bis(benzyloxy)benzaldehyde | HCID 79526 | — |
| 反応物 | 2-Amino-5-chloro-alpha-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol | HCID 54358865 | — |
| 反応物 | HCID 178511851 | HCID 178511851 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 2-(3,4-Dibenzyloxybenzyl)amino-5-chloro-alpha-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol | HCID 54423878 | 75.5% |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06352982B1 |
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| 出典データセット | uspto-grants-2002_03 |
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| ORD ID | ord-f1156755ca1643af932a9577860a226c |
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| 出典メモ | uspto-grants-2002_03 |
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