HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Pyridine → n-Fmoc-o-t-butyl-l-serinyl fluoride
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Pyridine | HCID 1049 | — |
| Edukt | Cyanuric fluoride | HCID 12664 | — |
| Edukt | N-(9-Fluorenylmethoxycarbonyl)-O-tert-butylserine | HCID 2724633 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | n-Fmoc-o-t-butyl-l-serinyl fluoride | HCID 11315144 | — |
Reaktionsschritte
N-FMOC-O-t-Butyl-L-serine (10 g, 26.07 mmol) (Bachem) was dissolved in dichloromethane (135 mL). Pyridine (2.11 mL, 26.07 mmol) (Aldrich) and cyanuric fluoride (3.52 g, 26.07 mmol) (Aldrich) were successively added at room temperature and the mixture was stirred overnight. Ice cold water (100 mL) was added and the resulting slurry was filtered. The filtrate was poured into a separatory funnel and the layers were separated. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to afford N-FMOC-O-t-butyl-L-serinyl fluoride as a colorless oil which solidified upon standing. (Yield 9.79 g., 97%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07084270B2 |
| Quelldatensatz | uspto-grants-2006_08 |
| ORD ID | ord-7e467cb3ee834f5c8c6a348a4e446e43 |
| Quellennotiz | uspto-grants-2006_08 |