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867044-28-8

867044-28-8 Structure

867044-28-8 Structure
IdentificationBack Directory
[Name]

9,10-Bis(2-naphthyl)anthracene-2-ylboronic acid
[CAS]

867044-28-8
[Synonyms]

9,10-Bis(2-naphthyl)
2-broate-9,10-di-2'naphthylanthracene
9,10-di(2-phthyl)anthracene-2-ylboronic acid
9,10-di-(Naphth-2-yl)anthracene-2-boronic acid
9,10-Bis(2-naphthyl)anthracene-2-ylboronic acid
9,10-Di(2-naphthyl)anthrace ne-2-yl boronic acid
9,10-BIS(NAPHTHALEN-2-YL)ANTHRACEN-2-YLBORONIC ACID
(9,10-Di(naphthalen-2-yl)anthracen-2-yl)boronic acid
(9,10-Di(naphthalen-2-yl)anthracen-3-yl)boronic acid
[9,10-bis(2-naphthalenyl)-2-anthracenyl]boronic acid
Boronic acid, (9,10-di-2-naphthalenyl-2-anthracenyl)-
BORONIC ACID,B-(9,10-DI-2-NAPHTHALENYL-2-ANTHRACENYL)-
(9,10-di-2-naphthalenyl-2-anthracenyl)- Boronic acid
[EINECS(EC#)]

1533716-785-6
[Molecular Formula]

C34H23BO2
[MDL Number]

MFCD11045063
[MOL File]

867044-28-8.mol
[Molecular Weight]

474.36
Chemical PropertiesBack Directory
[Boiling point ]

685.5±65.0 °C(Predicted)
[density ]

1.32±0.1 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Room Temperature
[pka]

8.43±0.30(Predicted)
Safety DataBack Directory
[HS Code ]

2931900090
Hazard InformationBack Directory
[Chemical Properties]

Yellow-green powder
[Synthesis]

2-Bromo-9,10-bis(2-naphthalenyl)anthracene

474688-76-1

Trimethyl borate

121-43-7

9,10-Bis(2-naphthyl)anthracene-2-ylboronic acid

867044-28-8

The general procedure for the synthesis of 9,10-bis(2-naphthalenyl)anthracene-2-boronic acid from 2-bromo-9,10-bis(2-naphthalenyl)anthracene and trimethyl borate was as follows: 2-bromo-9,10-bis(2-naphthalenyl)anthracene (10.00 g, 19.63 mmol, 1.0 eq.) was dissolved in THF (140 mL) according to the methodology described in EP13, and the solution was cooled to -78°C. At this temperature, n-butyllithium (2.5 M hexane solution, 10.2 mL, 25.52 mmol, 1.3 eq.) was slowly added dropwise, followed by stirring the reaction mixture for 2 hours. Next, trimethyl borate (6.12 g, 58.89 mmol, 3.0 eq.) was added at -78 °C and the reaction mixture was gradually warmed to room temperature. After the reaction was stirred continuously for 17 h, the reaction was quenched with hydrochloric acid solution, the resulting yellow precipitate was collected by filtration and washed with distilled water (2 x 30 mL). Finally, the resulting solid was dried under vacuum and used for subsequent reactions without further purification. Yield: 9.8 g (100%).

[References]

[1] Patent: US2016/211455, 2016, A1. Location in patent: Paragraph 0209; 0210; 0211
[2] Patent: US2008/125593, 2008, A1. Location in patent: Page/Page column 11-12
[3] Patent: EP1925618, 2008, A1. Location in patent: Page/Page column 15-16
[4] Patent: EP1970376, 2008, A1. Location in patent: Page/Page column 12-13
[5] Patent: EP2110373, 2009, A1. Location in patent: Page/Page column 18-19
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