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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Oxalic Acid | HCID 971 | — |
| Reactant | 4-Benzoyl-1-(5,6-dimethoxy-2-methylindol-3-ylglyoxyloyl)piperidine | HCID 13195540 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5,6-Dimethoxy-2-methyl-3-[2-(4-phenylhydroxymethylpiperidyl)-ethyl]indole oxalate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04101663 |
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| Source dataset | uspto-grants-1978_07 |
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| ORD ID | ord-35f6bac1de4d48f5a8a265ddf0aef5b8 |
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| Source note | uspto-grants-1978_07 |
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