HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 51263Erstellt: 25. Oktober 2026
Water → (2,3-Dimethoxyphenyl)(piperidin-4-yl)methanol
https://huagongshe.com/reaction/51263
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Toluene | HCID 1140 | — |
| Edukt | (2,3-Dimethoxyphenyl)(4-pyridinyl)methanol | HCID 314742 | — |
| Edukt | HCID 178418361 | HCID 178418361 | — |
| Katalysator | Rhodium | HCID 23948 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | (2,3-Dimethoxyphenyl)(piperidin-4-yl)methanol | HCID 10890362 | — |
Reaktionsschritte
A suitable inert reactor is charged with 4-[1-hydroxy-1-(2,3-dimethoxyphenyl)methyl]pyridine (10) (13.6 kg, 55.5 mol) as a toluene wet cake and 5% rhodium on carbon catalyst (2.7 kg, 50% wet with water) as a water wet cake at about 25° C. About 190 kg of methanol is added and the reactor is pressured to about 100 psig with hydrogen for about 4-12 hours at about 50° C. The catalyst is removed by filtration and the reactor and catalyst are rinsed with about 7 kg of methanol. Deionized water is used as a final wash of the catalyst wet cake. The reactor rinse filtrate and the reaction mixture filtrate are combined. The concentration of 4-[1-hydroxy-1-(2,3-dimethoxyphenyl)methyl]piperidine (11) is about 7 wt %, affording about 13 kg (90% average yield) of the title compound (11).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06713627B2 |
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| Quelldatensatz | uspto-grants-2004_03 |
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| ORD ID | ord-49f67a95f8fe42d4b3b03347ce6c57e7 |
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| Quellennotiz | uspto-grants-2004_03 |
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