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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484489Generated: October 30, 2026

2,6-Lutidine → Ethyl 4-(3-oxopropyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/484489

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-LutidineHCID 7937—
ReactantEthyl 4-(3-chloro-3-oxopropyl)-1-piperidinecarboxylateHCID 14989196—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-(3-oxopropyl)piperidine-1-carboxylateHCID 1498919781%

Reaction Steps

A mixture of 102 parts of ethyl 4-(3-chloro-3-oxopropyl)-1-piperidinecarboxylate, 45 parts of 2,6-dimethylpyridine and 630 parts of tetrahydrofuran was hydrogenated at normal pressure and at room temperature with 5 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated. The reside was dissolved in 650 parts of dichloromethane. The solution was washed twice with 100 parts of a hydrochloric acid solution 5% and twice with 100 parts of water, dried filtered and evaporated. The residue was distilled, yielding 71.1 parts (81%) of ethyl 4-(3-oxopropyl)-1-piperidinecarboxylate; bp. 130°-135° C. at 133 Pa (int. 46).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05231184
Source datasetuspto-grants-1993_07
ORD IDord-171b608a92034bdf8dd1f4bb141af203
Source noteuspto-grants-1993_07