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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858553Generated: November 3, 2026

HCID 22127314, compound → HCID 22128636, compound

https://huagongshe.com/reaction/1858553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22127314HCID 22127314—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 22128636HCID 2212863668%

Reaction Steps

A solution of 2.5 g (8.9 mmol) of (3RS,4RS)-1-benzyl-4-(p-tolyl)-piperidin-3-ol in 100 ml of methanol was hydrogenated at 5 bar at room temperature for 18 hours using a palladium (10%)-carbon catalyst. For the working up, the catalyst was filtered off, washed with methanol and the solution obtained was evaporated under reduced pressure. For purification, the residue was chromatographed on silica gel using a 5:1:0.1 mixture of methylene chloride, methanol and ammonia as the eluent. There were obtained 1.15 g (68% of theory) of (3RS,4RS)-4-(p-tolyl)-piperidin-3-ol as a colourless solid; MS: 191 (M)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06150526
Source datasetuspto-grants-2000_11
ORD IDord-3ae457b5d1f540b9826ed720dda50401
Source noteuspto-grants-2000_11