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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004932Generated: October 31, 2026

HCID 22127314, compound → HCID 22128636, compound

https://huagongshe.com/reaction/1004932

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 numberUS06051712
Source datasetuspto-grants-2000_04
ORD IDord-885d6de57b2c4ac490678c3e7550909f
Source noteuspto-grants-2000_04