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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2074327Generated: November 1, 2026

Tetrahydrofuran → 3-Pyridyl 4-(4-hydroxyphenoxy)-1-piperidinecarboxylate

https://huagongshe.com/reaction/2074327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant3-Pyridyl 4-[4-(benzyloxy)phenoxy]-1-piperidinecarboxylateHCID 67067055—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventIsopropanolHCID 3776—
Product3-Pyridyl 4-(4-hydroxyphenoxy)-1-piperidinecarboxylateHCID 6706707683.5%

Reaction Steps

10% Palladium-carbon (catalytic amount) was added to a THF (75 ml)/2-propanol (75 ml) solution containing 3-pyridyl 4-[4-(benzyloxy)phenoxy]-1-piperidinecarboxylate (3.7 g), and in a hydrogen gas atmosphere, this was stirred at room temperature under normal pressure for 24 hours. The catalyst was removed by filtration, and the filtrate was concentrated under reduced pressure, and the resulting solid was washed with EtOAc/hexane, and dried under reduced pressure to obtain 3-pyridyl 4-(4-hydroxyphenoxy)-1-piperidinecarboxylate (2.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919495B2
Source datasetuspto-grants-2011_04
ORD IDord-ecd666eb161f46589aef3084b9d3481a
Source noteuspto-grants-2011_04