Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Sulfur Dioxide | HCID 1119 | — |
| Reactant | Adamantane | HCID 9238 | — |
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Catalyst | Sodium orthovanadate | HCID 61671 | — |
| Catalyst | Bis(2,4-pentanedionato)vanadium(IV) Oxide | HCID 16217092 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Adamantanone | HCID 64151 | 7% |
Reaction Steps
A mixture of 2 mmol of adamantane, 0.2 mmol of N-hydroxyphthalimide, 0.01 mmol of vanadyl acetylacetonato [(VO (acac) 2 ], and 5 ml of acetic acid was stirred at 40° C. in a sulfur dioxide (SO2) (0.5 atm) and oxygen (0.5 atm) atmosphere for 2 hours. A gas chromatographic analysis of a reaction mixture revealed that the conversion rate of adamantane was 63% and that 2-adamantanone was formed in a yield of 7%. The reaction mixture was extracted with water, was neutralized with an aqueous sodium hydroxide solution, and was adjusted to weak acidity with hydrochloric acid. An aqueous benzyl isothiourea hydrochloride solution in large excess was then added to the mixture to separate S-benzyl thiuronium salt of 1-adamantanesulfonic acid. The yield of this compound was 40%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06143924 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-3f489a5ad76a491f817617e255042899 |
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| Source note | uspto-grants-2000_11 |
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