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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Benzyl-3-(3,4-dimethoxyphenyl)piperidin-3-ol | HCID 13066744 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13066745 | HCID 13066745 | 74.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04382942 |
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| Source dataset | uspto-grants-1983_05 |
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| ORD ID | ord-880b19d1a9c043e9b3422722945db92d |
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| Source note | uspto-grants-1983_05 |
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