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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451554Generated: October 31, 2026

Selectfluor → Tert-butyl 3-fluoro-4-oxopiperidine-1-carboxylate

https://huagongshe.com/reaction/451554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSelectfluorHCID 2724933—
Reactanttert-Butyl 4-((trimethylsilyl)oxy)-5,6-dihydropyridine-1(2H)-carboxylateHCID 10778540—
SolventAcetonitrileHCID 6342—
SolventSodium chloride; waterHCID 57417360—
ProductTert-butyl 3-fluoro-4-oxopiperidine-1-carboxylateHCID 10560711—

Reaction Steps

4-Trimethylsilyloxy-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester (13.2 g, 48.6 mmol) was dissolved in acetonitrile (250 mL). 1-Chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) (19.0 g, 53.5 mmol) was added and the reaction mixture was stirred at room temperature for 2 hours. Brine was added to the reaction mixture and the aqueous phase extracted ethyl acetate. The combined organic layers were dried over Na2SO4 and the solvent was evaporated. The residue was purified by flash chromatography (silica gel, 100 g, 0% to 100% EtOAc in heptane). The title compound was obtained as white solid (5.66 g, 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486967B2
Source datasetuspto-grants-2013_07
ORD IDord-271598a35ef146bc8a5ac51e69932705
Source noteuspto-grants-2013_07