HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 534678Erstellt: 26. Oktober 2026
Trifluoroacetic acid → N-benzyl-O-benzyl-D-serinamide
https://huagongshe.com/reaction/534678
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Trifluoroacetic acid | HCID 6422 | — |
| Edukt | N-benzyl-O-benzyl-N2-Boc-D-serinamide | HCID 7216909 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | N-benzyl-O-benzyl-D-serinamide | HCID 67082833 | 70% |
Reaktionsschritte
To a solution of N-benzyl-O-benzyl-N2-Boc-D-serinamide (3 g) and dichloromethane (15 mL), trifluoroacetic acid (15 mL) was added. The solution was stirred for 2 hours at 40° C. for completion of reaction. The solution was concentrated under vacuum to remove solvents and subsequently water was added. The aqueous layer was basified to pH 8-10 with 5% sodium hydroxide. The aqueous layer was extracted with ethyl acetate and the combined organic layer was washed with brine solution. Organic layer was concentrated under vacuum to obtain an oily residue solidify by n-Hexane to give 1.55 g of N-benzyl-O-benzyl-D-serinamide.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08853439B2 |
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| Quelldatensatz | uspto-grants-2014_10 |
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| ORD ID | ord-637b96a137da4747ae3a5d48b80551ca |
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| Quellennotiz | uspto-grants-2014_10 |
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