Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Selenium Dioxide | HCID 24007 | — |
| Reactant | 2-Acetylfluorenon | HCID 67615252 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-Fluorenonylglyoxal | HCID 86734632 | — |
Reaction Steps
The thus-isolated 2-acetylfluorenon is oxidized by selenium dioxide in dioxane medium at 98°-100° C during 22 hours to obtain 2-fluorenonyl-glyoxal isolated as semiacetal, the yield being equal to 31.2 weight percent. The thus-obtained intermediate product is subjected to treatment with sodium bisulfite in 60-percent ethanol to obtain the final product crystallizable with a molecule of water. The yield of the final product amounts to 57 weight percent when calculated for the semiacetal of 2-fluorenonyl-glyoxal and to 55 weight percent when calculated for the parent fluorene (of.Sintez organicheskikh preparatov/synthesis of organic preparations/, v.4, P.77, 1953 /in Russian/; Zhurnal organicheskoy khimii /Journal of organic chemistry/, 33, 3053, 1963 (in Russian).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04016289 |
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| Source dataset | uspto-grants-1977_04 |
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| ORD ID | ord-19b7dec615684202a30dc56823abd3cc |
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| Source note | uspto-grants-1977_04 |
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