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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030902Generated: October 30, 2026

Ethyl 4-(3-oxopropyl)piperidine-1-carboxylate → Ethyl 4-(3-hydroxypropyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1030902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-(3-oxopropyl)piperidine-1-carboxylateHCID 14989197—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-(3-hydroxypropyl)piperidine-1-carboxylateHCID 1498919898.3%

Reaction Steps

A mixture of 36 parts of ethyl 4-(3-oxopropyl)-1-piperidinecarboxylate and 450 parts of tetrahydrofuran was hydrogenated at normal pressure and at 20° C. with 2 parts of Raney nickel catalyst. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated. The residue was dissolved in 260 parts of dichloromethane. The organic layer was washed with 100 parts of a diluted hydrochloric acid solution, dried, filtered and evaporated, yielding 36 parts (98.3%) of ethyl 4-(3-hydroxypropyl)-1-piperidinecarboxylate as a residue (int. 47).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05106973
Source datasetuspto-grants-1992_04
ORD IDord-bdf0e28a851042c3992ff1e3a14ed70e
Source noteuspto-grants-1992_04