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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412246Generated: October 26, 2026

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

https://huagongshe.com/reaction/412246

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 stirred 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 my, yield; 60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562811B1
Source datasetuspto-grants-2003_05
ORD IDord-3e7be616785a4054b21c1eda668180ac
Source noteuspto-grants-2003_05