HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 232892Generated: November 1, 2026
Potassium Hydroxide → HCID 23361041, compound
https://huagongshe.com/reaction/232892
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 23361030 | HCID 23361030 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 23361041 | HCID 23361041 | 70% |
Reaction Steps
To a suspension of lithium aluminum hydride (114 mg, 3 mmol) and aluminum chloride (400 mg, 3 mmol) in ether (5 ml), a suspension of 1'-methylspiro[tetralin-2,3'-piperazine]-2',5'-dione (80 mg, 0.33 mmol) in ether (2 ml) was added, while the former was stirred under ice cooling conditions, followed by further stirring at room temperature for 10 minutes. After a 1N aqueous potassium hydroxide solution was added, the precipitate was filtered off. The filtrate was washed by sequential additions of a 1 N aqueous potassium hydroxide solution and chloroform. After the mother liquor was eluted with saturated saline, the organic layer was dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to yield the title compound (50 mg, 70%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05591849 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-6664de4d0f594402907c4e19aad889ba |
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| Source note | uspto-grants-1997_01 |
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