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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851131Generated: October 31, 2026

1-Benzyl-3-(3,4-dimethoxyphenyl)piperidin-3-ol → HCID 13066745, compound

https://huagongshe.com/reaction/851131

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-3-(3,4-dimethoxyphenyl)piperidin-3-olHCID 13066744—
ReactantHCID 178418361HCID 178418361—
SolventEthanolHCID 702—
ProductHCID 13066745HCID 1306674574.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 5 g of 10% palladized carbon and a solution of 9.8 g of N-benzyl-3-(3,4-dimethoxyphenyl)-3-hydroxy-piperidine [described in French patent No. 2,310,761] in 100 ml of ethanol was placed in an autoclave and hydrogen was introduced to obtain a pressure of 50 kg/cm2. The autoclave was sealed and was heated at 100° C. and the hydrogen pressure stabilized at 65 kg/cm2. The mixture was stirred at 100° C. for 32 hours and was then cooled and filtered. The filtrate was evaporated to dryness under reduced pressure and the residue was chromatographed over silica gel. Elution with a 75-20-5 chloroform-methanol-triethylamine mixture yielded 5.3 g of 3-(3,4-dimethoxyphenyl)-3-hydroxy-piperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04382942
Source datasetuspto-grants-1983_05
ORD IDord-880b19d1a9c043e9b3422722945db92d
Source noteuspto-grants-1983_05