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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489495Generated: October 25, 2026

Oxygen → 2,7Dibromofluorenone

https://huagongshe.com/reaction/489495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxygenHCID 977—
ReactantSodium HydroxideHCID 14798—
Reactant2,7-DibromofluoreneHCID 140073—
ReactantTetraammonium hydroxideHCID 21879771—
SolventTolueneHCID 1140—
Product2,7DibromofluorenoneHCID 5342010389.6%

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 a 25% aqueous solution of tetraammonium hydroxide (0.77 g) and a 48% aqueous solution of sodium hydroxide (2.66 g), the resulting mixture was vigorously stirred at 60° C. for 3 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 (8.26 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06977313B2
Source datasetuspto-grants-2005_12
ORD IDord-e4852cca99214f5da58148751d369d3c
Source noteuspto-grants-2005_12