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9-(3-Bromophenyl)-9-phenyl-9H-fluorene

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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
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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
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Safety Information

HS Code 
2903.99.8001
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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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