Identification | Back Directory | [Name]
9,9-diphenyl-9H-fluoreN-2-ylboronicacid | [CAS]
400607-31-0 | [Synonyms]
9,9-Diphenylfluoren-2-boronic acid 9,9-Diphenylfluorene-2-boronic acid 9,9-Diphenylfluoren-2-ylboronic acid 9,9-diphenyl-9h-fluoren-2-boronic acid 9,9-Diphenylfluorene-2-boronic Acid (c 9,9-diphenyl-9H-fluoreN-2-ylboronicacid 9,9-diphenyl-9H-fluoren-4-ylboronicacid 9,9-Diphenyl-9H-(fluorene-2-yl)-boronic acid Boronic acid, (9,9-diphenyl-9H-fluoren-2-yl)- B-(9,9-Diphenyl-9H-fluoren-2-yl)-boronic Acid Boronic acid,B-(9,9-diphenyl-9H-fluoren-2-yl)- 2,8-dibromo-6,6,12,12-tetramethyl-6H,12H-indeno[1,2-b]fluorene 9,9-Diphenylfluorene-2-boronic(containsvaryingamountsofAnhydride) 9,9-Diphenylfluorene-2-boronic Acid (contains varying amounts of Anhydride) | [Molecular Formula]
C25H19BO2 | [MDL Number]
MFCD22581299 | [MOL File]
400607-31-0.mol | [Molecular Weight]
362.228 |
Chemical Properties | Back Directory | [Boiling point ]
546.3±60.0 °C(Predicted) | [density ]
1.28±0.1 g/cm3(Predicted) | [storage temp. ]
Inert atmosphere,Room Temperature | [pka]
8.55±0.40(Predicted) | [Appearance]
White to off-white Solid |
Hazard Information | Back Directory | [Uses]
B-(9,9-Diphenyl-9H-fluoren-2-yl)-boronic Acid can be used to synthesize pyrrole/polycyclic aromatic units. It is a potential electroluminescent material. | [Synthesis]
General procedure for the synthesis of (9,9-diphenyl-9H-fluoren-2-yl)boronic acid from trimethyl borate and 2-bromo-9,9-diphenylfluorene: 10 g of 2-bromo-9,9-diphenylfluorene and 100 ml of anhydrous tetrahydrofuran were added to a 1-liter flask, and the mixture was cooled to -78 °C (using a bath of liquid nitrogen). Subsequently, 25.2 mL of n-butyllithium solution was added slowly and dropwise, followed by trimethyl borate. The reaction mixture was stirred at -78 °C and then allowed to warm naturally to room temperature. Then, an appropriate amount of dilute hydrochloric acid was added to carry out the hydrolysis reaction. Upon completion of the reaction, the mixture was extracted with ethyl acetate, the organic layer was separated and dried with anhydrous sodium sulfate. Finally, the solvent was removed by distillation under reduced pressure and the residue was eluted with hexane to afford 4 g of the target product (9,9-diphenyl-9H-fluoren-2-yl)boronic acid. | [References]
[1] Patent: CN106957272, 2017, A. Location in patent: Paragraph 0090; 0091 |
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