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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714211Generated: October 30, 2026

Nitrogen → tert-Butyl 3,3-difluoro-4-oxopiperidine-1-carboxylate

https://huagongshe.com/reaction/714211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantSodium SulfiteHCID 24437—
ReactantTriacetoxyperiodinaneHCID 159087—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-Butyl 3,3-difluoro-4-hydroxypiperidine-1-carboxylateHCID 56932106—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 3,3-difluoro-4-oxopiperidine-1-carboxylateHCID 56776981—

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), to an ice-cold solution of tert-butyl 3,3-difluoro-4-hydroxypiperidine-1-carboxylate (2.40 g, 10.00 mmol) in dry CH2Cl2 (50 mL) was added a solution of Dess-Martin periodinane (50 mL of a 15% solution in CH2Cl2, 24.00 mmol). The reaction mixture was stirred at rt until completion of the reaction. Sat. aq. NaHCO3 (50 mL) was then added followed by 10% aq. Na2SO3 (50 mL). The mixture was stirred at rt for 1 h, the layers separated and the aq. layer extracted with CH2Cl2 (3×). The combined org. extracts were dried over MgSO4, filtered, and concentrated under reduced pressure. The crude residue was redissolved in CH2Cl2 (30 mL) and stirred in the presence of molecular sieves for 24 h, filtered and concentrated under reduced pressure to give tert-butyl 3,3-difluoro-4-oxopiperidine-1-carboxylate as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187435B2
Source datasetuspto-grants-2015_11
ORD IDord-de32edbfea1547e3897c8cdf4ef9bb05
Source noteuspto-grants-2015_11