9,9-Dimethyl-9H-fluoren-2-yl-boronic acid CAS 333432-28-3

Introduction:Basic information about 9,9-Dimethyl-9H-fluoren-2-yl-boronic acid CAS 333432-28-3, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

9,9-Dimethyl-9H-fluoren-2-yl-boronic acid Basic information

Product Name:9,9-Dimethyl-9H-fluoren-2-yl-boronic acid
Synonyms:9,9-dimethyl-9h-fluoren-2-yl-boronic acid;BORONIC ACID,(9,9-DIMETHYL-9H-FLUOREN-2YL)-;Boronic acid, (9,9-dimethyl-9H-Fluoren-2-ylbutyl);9,9-DIMETHYL-9H-FLUOROEN-2-YL BORONIC ACID;9,9-DIMETHYL-2-FLUORENEBORONIC ACID;2-Bromo-9,9-dimethyl-9H-fluorene;9,9-dimethyl-9H-fluorene-2yl boronic acid;9,9-Dimethyl-9H-fluoren-2-yl-2-boronic acid
CAS:333432-28-3
MF:C15H15BO2
MW:238.09
EINECS:691-490-0
Product Categories:OLED materials,pharm chemical,electronic;Boron Compounds;Electronic Chemicals
Mol File:333432-28-3.mol

9,9-Dimethyl-9H-fluoren-2-yl-boronic acid Chemical Properties

Melting point 300 °C
Boiling point 436.5±48.0 °C(Predicted)
density 1.20±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form Solid
pka8.62±0.40(Predicted)
color White to Almost white
InChIInChI=1S/C15H15BO2/c1-15(2)13-6-4-3-5-11(13)12-8-7-10(16(17)18)9-14(12)15/h3-9,17-18H,1-2H3
InChIKeyDMDPAJOXRYGXCB-UHFFFAOYSA-N
SMILESB(C1C=CC2C3=C(C(C)(C)C=2C=1)C=CC=C3)(O)O

Safety Information

Hazard Codes Xi
Risk Statements 36
Safety Statements 26
HS Code 2931900090

9,9-Dimethyl-9H-fluoren-2-yl-boronic acid Usage And Synthesis

Chemical PropertiesOff-white powder
Uses9,9-Dimethyl-9h-fluoren-2-ylboronic acid
Synthesis

121-43-7

28320-31-2

333432-28-3

2-Bromo-9,9-dimethyl-9H-fluorene (100 g, 366 mmol) was dissolved in 1000 mL of tetrahydrofuran under nitrogen protection and cooled to -78 °C. At this temperature, a hexane solution of 1.6 M n-butyllithium (275 mL, 439 mmol) was slowly added dropwise. After the dropwise addition was completed, the reaction mixture was kept at -78 °C and continued to be stirred for 1 hour. Subsequently, the reaction mixture was slowly warmed to room temperature and trimethyl borate (49.5 g, 476 mmol) was added dropwise and stirring was continued for 1 hour at room temperature. Upon completion of the reaction, 1 M aqueous hydrochloric acid was added slowly and stirred for 30 minutes at room temperature. The organic layer was separated and concentrated under reduced pressure and the resulting crude product was recrystallized with a mixed solvent of dichloromethane and hexane to afford the title compound 9,9-dimethyl-2-boronic acid fluorene (70 g, 80% yield).

References[1] Patent: KR2015/114636, 2015, A. Location in patent: Paragraph 0730-0735
[2] Dyes and Pigments, 2013, vol. 96, # 3, p. 705 - 713
[3] Luminescence, 2015, vol. 30, # 5, p. 549 - 555
[4] Patent: WO2012/50371, 2012, A1. Location in patent: Page/Page column 12
[5] Patent: US2011/152587, 2011, A1. Location in patent: Page/Page column 13

9,9-Dimethyl-9H-fluoren-2-yl-boronic acid Preparation Products And Raw materials

Raw materialsTrimethyl borate-->Triisopropyl borate-->n-Butyllithium-->Tetrahydrofuran-->2-Bromo-9,9-dimethylfluorene
Preparation Products1-(9,9-Dimethylfluuoren-2-yl)isoquinoline
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