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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51264Generated: October 25, 2026

Methanol → (2,3-Dimethoxyphenyl)(piperidin-4-yl)methanol

https://huagongshe.com/reaction/51264

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTolueneHCID 1140—
Reactant(2,3-Dimethoxyphenyl)(4-pyridinyl)methanolHCID 314742—
ReactantHCID 178418361HCID 178418361—
CatalystRhodiumHCID 23948—
SolventAcetic AcidHCID 176—
Product(2,3-Dimethoxyphenyl)(piperidin-4-yl)methanolHCID 1089036296%

Reaction Steps

Into a suitable inerted reactor was charged 118 kg (481 mol) of 4-[1-hydroxy-1-(2,3-dimethoxyphenyl)methyl]pyridine (10) as a toluene wet cake and 23.6 kg of 5% rhodium on carbon catalyst at 25° C. To the slurry was then added 850 kg of methanol and 29 kg of glacial acetic acid. The reactor was then pressurized to about 100 psi with hydrogen for about 4-12 hours1 at 40° C. The catalyst was removed by filtration and the reactor and the catalyst were rinsed with 150 kg of methanol.2 The reactor rinse filtrate and the reaction mixture filtrate were combined. The concentration of 4-[1-hydroxy-1-(2,3-dimethoxyphenyl)methyl]piperidine (11) is typically about 10 wt %, affording about 116 kg of 4-[1-hydroxy-1-(2,3-dimethoxyphenyl)methyl]piperidine (11) (96% yield)3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713627B2
Source datasetuspto-grants-2004_03
ORD IDord-618235ac678c43d9af7c7634e866b26b
Source noteuspto-grants-2004_03