(9,9-Dimethyl-9H-fluoren-2,7-diyl)diboronic acid CAS 866100-14-3

Introduction:Basic information about (9,9-Dimethyl-9H-fluoren-2,7-diyl)diboronic acid CAS 866100-14-3, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

(9,9-Dimethyl-9H-fluoren-2,7-diyl)diboronic acid Basic information

Product Name:(9,9-Dimethyl-9H-fluoren-2,7-diyl)diboronic acid
Synonyms:BORONIC ACID, (9,9-DIMETHYL-9H-FLUORENE-2,7-DIYL)BIS;(9,9-dimethyl-9H-fluorene-2,7-diyl)bisboronic acid;Boronicacid,(9,9-dimethyl-9H-fluorene-2,7-diyl)b;(9,9-DIMETHYL-9H-FLUOROENE-2,7-DIYL)BISBORONIC ACID;(9,9-Dimethyl-9H-fluoren-2,7-diyl)diboronic acid;BORONIC ACID, (9,9-DIMETHYL-9H-FLUORENE-2,7-DIYL)BIS- (9CI);9,9-Dimethyl-9H-fluoren-2,7-diyl-2,7-diboronic acid;(9,9-Dimethyl-9H-flu
CAS:866100-14-3
MF:C15H16B2O4
MW:281.91
EINECS:805-314-9
Product Categories:OLED materrials;OLED materials,pharm chemical,electronic;Boron Compounds;Electronic Chemicals
Mol File:866100-14-3.mol

(9,9-Dimethyl-9H-fluoren-2,7-diyl)diboronic acid Chemical Properties

storage temp. Store at room temperature
AppearanceWhite to off-white Solid

Safety Information

HS Code 2931900090

(9,9-Dimethyl-9H-fluoren-2,7-diyl)diboronic acid Usage And Synthesis

Chemical PropertiesOff-white powder
Synthesis

5419-55-6

28320-32-3

866100-14-3

The general procedure for the synthesis of 9,9-dimethylfluorene-2,7-diboronic acid from triisopropyl borate and 2,7-dibromo-9,9-dimethylfluorene was as follows: 2,7-dibromo-9,9-dimethylfluorene (14.8 g, 42.4 mmol) was placed in a three-necked flask, 100 mL of tetrahydrofuran (THF) was added, and the reaction was cooled under nitrogen protection to -78 °C and maintained for 30 min. Subsequently, 21 mL of n-butyllithium (2.5 M) solution was added slowly and reacted for 1 hour. Next, triisopropyl borate (14 g) was added and the reaction was continued at low temperature for 1 hour, after which it was gradually warmed to room temperature. After completion of the reaction, the pH was adjusted to 4-5 by adding 2 M hydrochloric acid to the reaction mixture. the aqueous layer was extracted with ethyl acetate, the organic layers were combined and dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give Intermediate A1 (9.5 g, 80% yield).

References[1] Patent: CN106699780, 2017, A. Location in patent: Paragraph 0047; 0048; 0049; 0050
[2] Patent: US8058450, 2011, B2. Location in patent: Page/Page column 43-44
[3] Luminescence, 2015, vol. 30, # 5, p. 549 - 555

(9,9-Dimethyl-9H-fluoren-2,7-diyl)diboronic acid Preparation Products And Raw materials

Raw materialsTriisopropyl borate-->Hydrochloric acid-->2,7-Dibromo-9,9-dimethylfluorene-->Tetrahydrofuran-->n-Butyllithium
(9-(4-BROMOPHENYL))-9H-CARBAZOLE CAS 57102-42-8
(9-phenyl-9H-carbazol-2-yl)boronic acid CAS 1001911-63-2
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