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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486444Generated: October 30, 2026

Thiophene → HCID 67823130, compound

https://huagongshe.com/reaction/486444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiopheneHCID 8030—
ReactantPotassium AcetateHCID 517044—
ReactantHCID 19095528HCID 19095528—
ReactantHCID 178418361HCID 178418361—
ReactantHCID 178486302HCID 178486302—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 67823130HCID 6782313075%

Reaction Steps

A mixture of 21 parts of N-(3-methylphenyl)-1-(phenylmethyl)-4-piperidinamine dihydrochloride, 9 parts of poly(oxymethylene), 15 parts of potassium acetate, 2 parts of a solution of thiophene in methanol 4% and 200 parts of methanol was hydrogenated at normal pressure and at room temperature with 4 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off over Hyflo and the filtrate was evaporated. From the residue, the free base was liberated with ammonium hydroxide and extracted with dichloromethane. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (99:1 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was converted into the hydrochloride salt in 2-propanol. The salt was filtered off and dried, yielding 2.4 parts (75%) of N-methyl-N-(3-methylphenyl)-1-(phenylmethyl)-4-piperidinamine dihydrochloride hemihydrate; mp. 201.3° C. (intermediate 96).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05292738
Source datasetuspto-grants-1994_03
ORD IDord-f55f328eba7d4f46a9f7f897a671df88
Source noteuspto-grants-1994_03