Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Idramantone | HCID 64184 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | 4-Aminoadamantan-1-ol | HCID 2857447 | — |
Reaction Steps
To a solution of 5-hydroxy-2-adamantanone (10.2 g) in 8M ammonia (in methanol, 50 ml), 10% palladium on activated carbon (1.00 g) was added and stirred under a hydrogen atmosphere at room temperature for 15 hours. After the reaction mixture was filtered, the solvent was distilled off under reduced pressure and the resulting residue was purified by NH silica gel column chromatography (eluting solvent: chloroform alone→chloroform:methanol=9:1) to give 4-aminoadamantan-1-ol (10.2 g, E-form:Z-form=4:1). 4-Aminoadamantan-1-ol thus obtained (10.2 g) was dissolved by heating in tetrahydrofuran (50 ml), and 4M hydrochloric acid (in 1,4-dioxane, 20 ml) was added thereto, followed by stirring at room temperature for 16 hours. The precipitated solid was collected by filtration to give 4-aminoadamantan-1-ol hydrochloride (12.1 g, E-form:Z-form=4:1). The resulting E/Z mixture (9.15 g) was dissolved by heating in ethanol (450 ml) and water (35.5 ml), and stirred at room temperature for 2 days. The precipitated solid was collected by filtration to give the titled compound, i.e., E-4-aminoadamantan-1-ol hydrochloride (3.59 g) as a colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08222417B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-6912dc4362334dbf9e15bd3efda9a6cd |
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| Source note | uspto-grants-2012_07 |
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