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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43648Generated: October 26, 2026

Di-tert-butyl dicarbonate → Tert-butyl 3-ethoxy-4-oxopiperidine-1-carboxylate

https://huagongshe.com/reaction/43648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantTrifluoroacetic acid waterHCID 22392675—
ReactantTert-butyl 3-ethoxy-4,4-dimethoxypiperidine-1-carboxylateHCID 68406637—
ProductTert-butyl 3-ethoxy-4-oxopiperidine-1-carboxylateHCID 6840617795.5%

Reaction Steps

The same operation as in Example (90b) was performed using tert-butyl 3-ethoxy-4,4-dimethoxypiperidine-1-carboxylate obtained in Example (112a) (4.99 g, 14.2 mmol), a water/TFA mixed solution (1/1, 35 mL) and di-tert-butyl dicarbonate (4.37 g, 20 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 3.3 g of the title compound as a light brown oily substance (77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536197B2
Source datasetuspto-grants-2013_09
ORD IDord-db4db5c93845483ab2bd2f99b586a6ad
Source noteuspto-grants-2013_09