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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115673Generated: October 29, 2026

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

https://huagongshe.com/reaction/2115673

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 mg, yield; 60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435743B2
Source datasetuspto-grants-2008_10
ORD IDord-c7e4b21242734a2081cae12f56242e3f
Source noteuspto-grants-2008_10