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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004984Generated: November 3, 2026

HCID 22126993, compound → HCID 22128196, compound

https://huagongshe.com/reaction/1004984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22126993HCID 22126993—
CatalystHCID 57448735HCID 57448735—
SolventEthanolHCID 702—
ProductHCID 22128196HCID 2212819679%

Reaction Steps

A solution of 2.0 g (6.72 mmol) of (3RS,4RS)-l-benzyl-4-(4-hydroxymethyl-phenyl)-piperidin-3-ol in 100 ml of ethanol was hydrogenated at room temperature and 3 bar for 4 hours in the presence of 1.0 g of palladium oxide/charcoal (20%). For the working-up, the catalyst was filtered off under suction over Dicalit and the residue was washed twice with 50 ml of ethanol each time. The ethanol solution was evaporated under reduced pressure and the residue was chromatographed on silica gel using a 65:10:1 mixture of methylene chloride, methanol and ammonia as the eluent. There were obtained 1.1 g (79% of theory) of (3RS,4RS)-4-(4-hydroxymethyl-phenyl)-piperidin-3-ol as a colourless solid; MS: 207 (M)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06051712
Source datasetuspto-grants-2000_04
ORD IDord-ed0e638efccb46298adeca8cccc479f9
Source noteuspto-grants-2000_04