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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433175Generated: October 31, 2026

Pyridine → 2-Bromo-9-fluorenone

https://huagongshe.com/reaction/1433175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-Bromo-9H-fluoreneHCID 14336—
ReactantTetrabutylammonium HydroxideHCID 2723671—
SolventAcetic AcidHCID 176—
Product2-Bromo-9-fluorenoneHCID 725831—

Reaction Steps

9.8 g (40 mmol) of 2-bromofluorene, 40 mL of pyridine, and 1.5 mL of tetrabutylammonium hydroxide (1.0 mol/1 methanol solution) were put into a 200 mL three-neck flask. This solution was stirred under air at room temperature for 24 hours. After completion of a reaction, 40 m/L of glacial acetic acid was added to the reaction solution and stirred for 1 hour. Then, the reaction solution was washed with water and a water layer was extracted with ethyl acetate. The extracted solution and an organic layer were combined and washed with saturated saline, and then dried with magnesium sulfate. After drying, this mixture was subjected to suction filtration, and a filtrate was concentrated. When an obtained solid was recrystallized with ethanol, 7.9 g of a yellow, powdery solid of 2-bromo-9-fluorenone that was a target matter was obtained with the yield of 76%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612204B2
Source datasetuspto-grants-2009_11
ORD IDord-9bd9d604810347c3858f16f200c1ba4b
Source noteuspto-grants-2009_11