9-(3-Bromophenyl)-9-phenyl-9H-fluorene
9-(3-Bromophenyl)-9-phenyl-9H-fluorene Basic information
- Product Name:
- 9-(3-Bromophenyl)-9-phenyl-9H-fluorene
- Synonyms:
-
- 9-(3-Bromophenyl)-9-phenyl-9H-fluorene
- 9-(3-bromophenyl)-9-phenyl-9H-fluoren
- 9-(3-Bromophenyl)-9-phenyl-fluorene
- 3-BPF
- 9H-Fluorene, 9-(3-bromophenyl)-9-phenyl-
- 9-(3-Bromophenyl)-9-phenyl-9H-fluorene ISO 9001:2015 REACH
- CAS:
- 1257251-75-4
- MF:
- C25H17Br
- MW:
- 397.31
- Mol File:
- 1257251-75-4.mol
9-(3-Bromophenyl)-9-phenyl-9H-fluorene Chemical Properties
- Melting point:
- 131.0 to 135.0 °C
- Boiling point:
- 480.5±24.0 °C(Predicted)
- Density
- 1.363±0.06 g/cm3(Predicted)
- solubility
- soluble in Toluene
- form
- powder to crystal
- color
- White to Almost white
- CAS DataBase Reference
- 1257251-75-4
9-(3-Bromophenyl)-9-phenyl-9H-fluorene Usage And Synthesis
Uses
9-(3-Bromophenyl)-9-phenyl-9H-fluorene is a useful research chemical.
Description
9-(3-Bromophenyl)-9-phenyl-9H-fluorene (9-(3-bromophenyl)-9-phenylfluorene) is an important organic intermediate to synthetize its substituted products.
Synthesis
A solution of 10.0 g of 2-bromobiphenyl (42.9 mmol) in 70 ml of anhydrous THF was added to a 500 mE 3-neck flask and cooled to -78 C. 27 ml of a 1.58 M hexane solution of n-BuEi (42.9 mmol) was then added dropwise while stirring, and the reaction was stirred for about 2.5 hours. A solution of 9.30 g (35.6 mmol) of 3-bromobenzophenone in 85 mE of an anhydrous THF was added dropwise, and the resulting mixture was stirred for about 2 hours at -78 C. followed by stirring for about 3 hours at room temperature. 1 N hydrochloric acid (HC1) was then added to the mixture and stirred for about 1 hour. The mixture was washed with water, and the resultant organic phase was concentrated to afford a material having a candy-like consistency. The candy-like material, 50 ml of acetic acid, and 2.4 ml of hydrochloric acid were added to a 500 mL recovery flask, and the mixture was stirred and reacted at 130 C. under a nitrogen atmosphere for about 2 hours. After the reaction, the reaction mixture was added dropwise to 350 ml of ice-cold water, precipitating white crystals, and the crystals were isolated by filtration. The crystals were washed with methanol and allowed to dry. About 13.3 g of Compound A was obtained as a white powder (yield: about 78%).
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