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654664-63-8

654664-63-8 Structure

654664-63-8 Structure
IdentificationBack Directory
[Name]

B-2-Triphenylenylboronic acid
[CAS]

654664-63-8
[Synonyms]

triphenylen-2-ylboronic
2-tripheylenylboronic acid
2-Triphenylenylboronic acid
Triphenylene-2-boronic acid
2-Triphenylene boronic acid
Triphenylen-2-ylboronic acid
B-2-Triphenylenylboronic acid
B-2-Triphenylene boronic acid
Boronic acid, 2-triphenylenyl-
triphenylene-2-yl boronic acid
Boronic acid, B-2-triphenylenyl-
Triphenylen-2-ylboronic acid 98%
9,10-BenzophenanthreN-2-ylboronicacid
9,10-Benzophenanthrene-2-yl-boronic acid
TIANFU-CHEM 654664-63-8 B-2-Triphenylenylboronic acid
Triphenylen-2-ylboronic acid/ B-2-Triphenylenylboronic acid
[EINECS(EC#)]

1533716-785-6
[Molecular Formula]

C18H13BO2
[MDL Number]

MFCD16660186
[MOL File]

654664-63-8.mol
[Molecular Weight]

272.11
Chemical PropertiesBack Directory
[Boiling point ]

565.5±33.0 °C(Predicted)
[density ]

1.30
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[pka]

8.53±0.30(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P280-P301+P312-P362+P364
[HS Code ]

2931900090
Hazard InformationBack Directory
[Chemical Properties]

Yellow solid
[Synthesis]

Trimethyl borate

121-43-7

2-bromobenzo[9,10]phenanthrene

19111-87-6

B-2-Triphenylenylboronic acid

654664-63-8

The general procedure for the synthesis of 2-triphenylenylboronic acid from trimethyl borate and 2-bromobenzo[9,10]phenanthrene was carried out as follows: the intermediate E1 (2.90 g, 9.44 mmol) was dissolved in tetrahydrofuran (80 ml) under argon protection and cooled to -78 °C. Subsequently, n-BuLi (1.60 M hexane solution, 6.20 ml, 9.11 mmol) was slowly added and gradually warmed to 0 °C over 2 h. The reaction mixture was then cooled to -78 °C under argon protection. The reaction mixture was again cooled to -78 °C, trimethoxyborane (2.58 g, 24.8 mmol) was added and stirred at -78 °C for 20 minutes before slowly warming to room temperature and continuing to stir for 8 hours. After completion of the reaction, 1M aqueous hydrochloric acid (20 ml) was added and stirred at room temperature for 1 hour. The organic layer was extracted with ethyl acetate, the organic phases were combined and dried with magnesium sulfate. After concentration, the residue was dissolved in hexane and purified by suspension, washing, filtration and recrystallization to give intermediate E2 (1.46 g, 5.38 mmol, 57% yield).

[References]

[1] Patent: CN105473600, 2016, A. Location in patent: Paragraph 0184; 0185
[2] Patent: CN105431441, 2016, A. Location in patent: Paragraph 0152; 0153; 0154
[3] Patent: US2011/54228, 2011, A1. Location in patent: Page/Page column 8
[4] Patent: US2017/162796, 2017, A1. Location in patent: Paragraph 0166; 0167
Spectrum DetailBack Directory
[Spectrum Detail]

B-2-Triphenylenylboronic acid(654664-63-8)1HNMR
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