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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767334Generated: October 25, 2026

Tert-butyl 3-(2-methoxyethenyl)-1-piperidinecarboxylate → tert-Butyl 3-(2-oxoethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1767334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 3-(2-methoxyethenyl)-1-piperidinecarboxylateHCID 69249758—
SolventFormic AcidHCID 284—
Producttert-Butyl 3-(2-oxoethyl)piperidine-1-carboxylateHCID 2225894760%

Reaction Steps

tert-Butyl 3-(2-methoxyethenyl)-1-piperidinecarboxylate (1.16 g, 4.81 mmol) was dissolved in 90% formic acid (2 mL). The mixture was stiffed at room temperature for 40 min. The mixture was then partitioned between ethyl acetate and saturated aqueous NaHCO3 solution. The separated organic phase was washed with brine, dried over Na2SO4, filtered and evaporated. Purification by column chromatography (hexane/ethyl acetate=4/1) gave tert-butyl 3-(2-oxoethyl)-1-piperidinecarboxylate as a colorless oil (652 mg, yield; 60%). [Starting Compound 2H]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07232909B2
Source datasetuspto-grants-2007_06
ORD IDord-4d6a3f7440d44da0940eeac6a7c366f5
Source noteuspto-grants-2007_06