HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 275866Erstellt: 26. Oktober 2026
Acetic Acid → 2-[2-(4-Benzyloxyphenyl)ethyl]amino-alpha-(3-tert-butoxycarbonylaminomethylphenyl)-5-chloro-benzyl alcohol
https://huagongshe.com/reaction/275866
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | 4-Benzyloxyphenylacetaldehyde | HCID 11413489 | — |
| Edukt | 2-Amino-5-chloro-alpha-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol | HCID 54358865 | — |
| Edukt | HCID 178511852 | HCID 178511852 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 2-[2-(4-Benzyloxyphenyl)ethyl]amino-alpha-(3-tert-butoxycarbonylaminomethylphenyl)-5-chloro-benzyl alcohol | HCID 54258279 | — |
Reaktionsschritte
In methanol (15 ml) were dissolved 2-amino-5-chloro-α-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol produced in Example 1-(2) (0.5 g) and 4-benzyloxyphenylacetaldehyde (0.4 g). To the solution were added acetic acid (0.1 g) and, subsequently, cyano sodium hydride (0.11 g). The mixture was stirred for 40 minutes at 60° C. The reaction mixture was diluted with ethyl acetate (60 ml), which was washed with water and dried over anhydrous sodium sulfate. The solvent was distilled off to leave 2-[2-(4-benzyloxyphenyl)ethyl]amino-α-(3-tert-butoxycarbonylaminomethylphenyl)-5-chloro-benzyl alcohol (0.45 g) as a colorless oily product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06352982B1 |
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| Quelldatensatz | uspto-grants-2002_03 |
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| ORD ID | ord-1c8c5b7df28743a49d051f48e5d4a748 |
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| Quellennotiz | uspto-grants-2002_03 |
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