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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071564Generated: October 31, 2026

Oxalic Acid → 5,6-Dimethoxy-2-methyl-3-[2-(4-phenylhydroxymethylpiperidyl)-ethyl]indole oxalate

https://huagongshe.com/reaction/2071564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalic AcidHCID 971—
Reactant4-Benzoyl-1-(5,6-dimethoxy-2-methylindol-3-ylglyoxyloyl)piperidineHCID 13195540—
ReactantAluminium lithium hydrideHCID 21226445—
SolventIsopropanolHCID 3776—
SolventTetrahydrofuranHCID 8028—
Product5,6-Dimethoxy-2-methyl-3-[2-(4-phenylhydroxymethylpiperidyl)-ethyl]indole oxalateHCID 20311694—

Reaction Steps

A suspension of 20.2 g of 4-benzoyl-1-(5,6-dimethoxy-2-methylindol-3-ylglyoxyloyl)piperidine in 200 ml of tetrahydrofuran is added dropwise to a stirring solution, under nitrogen at a reflux, of 9.6 g of lithium aluminum hydride in 210 ml of tetrahydrofuran. Stirring and refluxing is continued for 3 hours, the mixture is cooled in an ice bath and the excess hydride is destroyed with water. The mixture is filtered and the filtrate is concentrated under reduced pressure, leaving an off-white foam which is triturated with cyclohexane to give an off-white powder. The oxalate salt is prepared by dissolving the free base in isopropanol and slowly adding a solution of oxalic acid in isopropanol. The insoluble oxalate salt is collected and recrystallized from ethanol to give white crystals, mp 152°-154° C., 5,6-dimethoxy-2-methyl-3-[2-(4-phenylhydroxymethylpiperidyl)ethyl]indole oxalate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04046900
Source datasetuspto-grants-1977_09
ORD IDord-19d3f7a45a094f919a75da86b9e19eed
Source noteuspto-grants-1977_09