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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2074268Generated: November 1, 2026

Tetrahydrofuran → HCID 67067094, compound

https://huagongshe.com/reaction/2074268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 67067073HCID 67067073—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventIsopropanolHCID 3776—
ProductHCID 67067094HCID 6706709470.8%

Reaction Steps

10% Palladium-carbon (catalytic amount) was added to a THF (75 ml)/2-propanol (75 ml) solution containing 3-pyridyl 4-[3-(benzyloxy)phenoxy]-1-piperidinecarboxylate (4.0 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-(3-hydroxyphenoxy)-1-piperidinecarboxylate (2.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919494B2
Source datasetuspto-grants-2011_04
ORD IDord-6f6229fbba7f407ba7cc6f95488e6fd7
Source noteuspto-grants-2011_04