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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7234Generated: October 25, 2026

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

https://huagongshe.com/reaction/7234

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantCyanuric fluorideHCID 12664—
ReactantN-(9-Fluorenylmethoxycarbonyl)-O-tert-butylserineHCID 2724633—
SolventDichloromethaneHCID 6344—
Productn-Fmoc-o-t-butyl-l-serinyl fluorideHCID 11315144—

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07084270B2
Source datasetuspto-grants-2006_08
ORD IDord-7e467cb3ee834f5c8c6a348a4e446e43
Source noteuspto-grants-2006_08