| Identification | Back Directory | [Name]
3-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-carbazole | [CAS]
855738-89-5 | [Synonyms]
3-Boronic acid pinacol carbazole 3-carbazoleboronic acid pinacolate Carbazole-3-boronic Acid Pinacol Ester 3- Frequency boric acid ester carbazole 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan 9H-Carbazole-3-boronic acid pinacol ester (9H-CARBAZOL-3-YL)BORONIC ACID PINACOL ESTER 3-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-carbazole 3-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-9H-Carbazole 2-(9H-Carbazol-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 9H-Carbazole, 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- | [Molecular Formula]
C18H20BNO2 | [MDL Number]
MFCD16996081 | [MOL File]
855738-89-5.mol | [Molecular Weight]
293.168 |
| Chemical Properties | Back Directory | [Melting point ]
194.0 to 198.0 °C | [Boiling point ]
474.3±18.0 °C(Predicted) | [density ]
1.16±0.1 g/cm3(Predicted) | [storage temp. ]
Inert atmosphere,2-8°C | [form ]
powder to crystal | [pka]
16.76±0.30(Predicted) | [color ]
White to Orange to Green | [CAS DataBase Reference]
855738-89-5 |
| Hazard Information | Back Directory | [Chemical Properties]
off-white powder | [Synthesis]
1,1'-Bis(diphenylphosphino)ferrocene palladium dichloride dichloromethane complex (0.2 g, 0.25 mmol) and potassium acetate (1.5 g) were added to a 100 mL double-necked vial with 3-bromocarbazole (1 g, 5.98 mmol) and bis(diphenylphosphino)pinacol bis(boronic acid) ester (1.52 g, 5.98 mmol). 1,4-dioxane (40 mL) and a magnetic stirrer were then added and a reflux condenser tube was installed. The system was evacuated by vacuum and then displaced three times with nitrogen and the reaction was carried out in an oil bath at 80°C for 24 hours. Upon completion of the reaction, two extractions with dichloromethane and water were performed, and the organic phases were combined and dried with anhydrous sodium sulfate. The target product 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)carbazole was purified by column chromatography (eluent ratio of petroleum ether: dichloromethane: ethyl acetate = 20:2:1) in 99% yield. | [References]
[1] Patent: CN104650153, 2017, B. Location in patent: Paragraph 0036; 0037; 0038; 0039 [2] Patent: KR2015/68182, 2015, A. Location in patent: Paragraph 0097-0099; 0107-0109 [3] Patent: JP2015/6995, 2015, A. Location in patent: Paragraph 0132 [4] Patent: CN106046054, 2016, A. Location in patent: Paragraph 0068; 0069 |
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