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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280377Generated: October 31, 2026

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

https://huagongshe.com/reaction/2280377

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantEthyl AcetateHCID 8857—
ReactantSelectfluorHCID 2724933—
Reactanttert-Butyl 4-((trimethylsilyl)oxy)-5,6-dihydropyridine-1(2H)-carboxylateHCID 10778540—
SolventAcetonitrileHCID 6342—
ProductTert-butyl 3-fluoro-4-oxopiperidine-1-carboxylateHCID 10560711—

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), to a solution of tert-butyl 4-((trimethylsilyl)oxy)-5,6-dihydropyridine-1(2H)-carboxylate (5.00 g, 18.40 mmol) in dry acetonitrile (25 mL) was added Selectfluor® (7.55 g, 20.3 mmol) at rt. The reaction mixture was stirred at rt for 2 h then poured into EA and successively washed with aq. 1% NaHCO3 and brine. The org. layer was dried over MgSO4, filtered, and concentrated under reduced pressure. The residue was purified by FC (hexanes/EA, 4:1) to afford the title compound as a pale yellow solid. LC-MS-conditions 08: tR=0.55 min; [M-CH3+H]+=203.23; TLC: rf (hexanes/EA, 4:1)=0.17.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139524B2
Source datasetuspto-grants-2015_09
ORD IDord-fb3ce4ad9c124b35b754e6b0acbe4916
Source noteuspto-grants-2015_09