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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867027Generated: October 30, 2026

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

https://huagongshe.com/reaction/867027

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 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 numberUS04101663
Source datasetuspto-grants-1978_07
ORD IDord-35f6bac1de4d48f5a8a265ddf0aef5b8
Source noteuspto-grants-1978_07