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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7234Erstellt: 23. Oktober 2026

Pyridine → n-Fmoc-o-t-butyl-l-serinyl fluoride

https://huagongshe.com/de/reaction/7234

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktCyanuric fluorideHCID 12664—
EduktN-(9-Fluorenylmethoxycarbonyl)-O-tert-butylserineHCID 2724633—
LösungsmittelDichloromethaneHCID 6344—
Produktn-Fmoc-o-t-butyl-l-serinyl fluorideHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07084270B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-7e467cb3ee834f5c8c6a348a4e446e43
Quellennotizuspto-grants-2006_08