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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489499Generated: October 30, 2026

Oxygen → 2,7Dibromofluorenone

https://huagongshe.com/reaction/489499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxygenHCID 977—
ReactantSodium HydroxideHCID 14798—
Reactant2,7-DibromofluoreneHCID 140073—
CatalystTetraammonium bromideHCID 22266889—
SolventTolueneHCID 1140—
Product2,7DibromofluorenoneHCID 5342010384.9%

Reaction Steps

Into a three-necked, 300-mL flask equipped with a stirrer, a molecular-oxygen-containing gas (air) inlet tube and a gas outlet tube (fitted with a condenser), 2,7-dibromofluorene (9.30 g, 0.029 mol) was charged, followed by its dissolution with toluene (100 g). Subsequent to addition of tetraammonium bromide (0.24 g) and a 48% aqueous solution of sodium hydroxide (2.66 g), the resulting mixture was vigorously stirred at 40° C. for 5 hours while introducing air at a flow rate of 0.1 L/min. After completion of the stirring, the reaction mixture was allowed to stand, and the resulting toluene layer was collected. The toluene layer was then subjected to acid washing, followed by water washing until its pH arose to 7. Toluene was then distilled off to recover crude crystals of 2,7-dibromofluorenone. The content of 2,7-dibromofluorene in the crude crystals at that time was 0%. Those crude crystals were recrystallized from N,N′-dimethylformamide (15 g) to afford 2,7-dibromofluorenone as yellow crystals (7.83 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06977313B2
Source datasetuspto-grants-2005_12
ORD IDord-2fc5b641f20446ff90d94f0f6c239f25
Source noteuspto-grants-2005_12