Identification | Back 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 Properties | Back 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 |
Hazard Information | Back Directory | [Chemical Properties]
Yellow solid | [Synthesis]
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 |
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