Participants
| Role | Name | HCID | Charge |
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| Reactant | Oxygen | HCID 977 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,7-Dibromofluorene | HCID 140073 | — |
| Catalyst | Tetraammonium bromide | HCID 22266889 | — |
| Product | 2,7Dibromofluorenone | HCID 53420103 | 83.2% |
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 “Cactus Solvent P-150” (product of Nikko Petrochemicals Co., Ltd.; 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 60° C. for 2 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 “Cactus Solvent P-150” layer was collected. The “Cactus Solvent P-150” layer was then subjected to acid washing, followed by water washing until its pH arose to 7. “Cactus Solvent P-150” 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 (7.67 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06977313B2 |
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| Source dataset | uspto-grants-2005_12 |
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| ORD ID | ord-9b5daf01d0b845058bb5d33b2daa94f7 |
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| Source note | uspto-grants-2005_12 |
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