Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1425172Generated: October 26, 2026

Di-tert-butyl dicarbonate → tert-Butyl 3-(2-fluoroethoxy)-4-oxopiperidine-1-carboxylate

https://huagongshe.com/reaction/1425172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDi-tert-butyl dicarbonateHCID 90495—
Reactanttert-Butyl 3-(2-fluoroethoxy)-4,4-dimethoxypiperidine-1-carboxylateHCID 86648640—
SolventTrifluoroacetic acid waterHCID 22392675—
Producttert-Butyl 3-(2-fluoroethoxy)-4-oxopiperidine-1-carboxylateHCID 8664864197.5%

Reaction Steps

The same operation as in Example (90b) was performed using tert-butyl 3-(2-fluoroethoxy)-4,4-dimethoxypiperidine-1-carboxylate obtained in Example (123a) (6.5 g, 21.2 mmol), a water/TFA mixed solution (1/1, 20 mL) and di-tert-butyl dicarbonate (6.54 g, 30 mol). The resulting residue was purified by silica gel column chromatography (elution solvent: hexane/ethyl acetate=10/1, 5/1, 2/1, 1/1) to obtain 5.4 g of the title compound as a light brown oily substance (98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927588B2
Source datasetuspto-grants-2015_01
ORD IDord-b0858013651b4ba7a5fc5638b51cc416
Source noteuspto-grants-2015_01