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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973818Generated: November 2, 2026

Methanol → HCID 86734311, compound

https://huagongshe.com/reaction/1973818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant2-IndanoneHCID 11983—
ReactantNorcarfentanilHCID 2724431—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
ProductHCID 86734311HCID 86734311—

Reaction Steps

A mixture of 2 parts of 1,3-dihydro-2H-inden-2-one, 4.4 parts of methyl 4-[N-(1-oxopropyl)-N-phenylamino]-4-piperidinecarboxylate and 80 parts of methanol is hydrogenated at normal pressure and at room temperature with 2 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen is taken up, the catalyst is filtered off and the filtrate is evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and 5% of methanol as eluent. The pure fractions are collected and the eluent is evaporated. The residue is dissolved in 2,2'-oxybispropane. The solution is stirred with activated charcoal. The latter is filtered off and the filtrate is evaporated. The residue is converted into the ethanedioate salt in 4-methyl-2-pentanone. The salt is filtered off and crystallized from 2-propanol, yielding methyl 1-(2,3-dihydro-1H-inden-2-yl)-4-[N-(1-oxopropyl)-N-phenylamino]-4-piperidinecarboxylate ethanedioate 2-propanolate; mp. 206° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03998834
Source datasetuspto-grants-1976_12
ORD IDord-73f1840c0dea4a55a7a4aac9f060d40d
Source noteuspto-grants-1976_12