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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328241Generated: October 26, 2026

Selenium Dioxide → 2-Fluorenonylglyoxal

https://huagongshe.com/reaction/328241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSelenium DioxideHCID 24007—
Reactant2-AcetylfluorenonHCID 67615252—
Solvent1,4-DioxaneHCID 31275—
Product2-FluorenonylglyoxalHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04016289
Source datasetuspto-grants-1977_04
ORD IDord-19b7dec615684202a30dc56823abd3cc
Source noteuspto-grants-1977_04