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| | (3-(carbazole-9H)Phenyl)Pinacol ester Basic information | | Uses |
| Product Name: | (3-(carbazole-9H)Phenyl)Pinacol ester | | Synonyms: | (3-(carbazole-9H)Phenyl)Pinacol ester;9-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-9H-carbazole;9H-Carbazole,9-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-;9-(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbazole;(3-(carbazole-9H)Phenyl)Picol ester;(3-(car;(3-(Carbazole-9H)Phenyl)Pinacol Ester,>98%;3-(9H-Carbazol-9-yl)phenylboronic acid pinacol ester | | CAS: | 870119-58-7 | | MF: | C24H24BNO2 | | MW: | 369.27 | | EINECS: | | | Product Categories: | | | Mol File: | 870119-58-7.mol |  |
| | (3-(carbazole-9H)Phenyl)Pinacol ester Chemical Properties |
| Melting point | 128.0 to 132.0 °C | | Boiling point | 483.2±37.0 °C(Predicted) | | density | 1.11±0.1 g/cm3(Predicted) | | storage temp. | under inert gas (nitrogen or Argon) at 2-8°C | | form | powder to crystal | | color | White to Almost white | | InChI | InChI=1S/C24H24BNO2/c1-23(2)24(3,4)28-25(27-23)17-10-9-11-18(16-17)26-21-14-7-5-12-19(21)20-13-6-8-15-22(20)26/h5-16H,1-4H3 | | InChIKey | YWLGYAZJWNLVKB-UHFFFAOYSA-N | | SMILES | C1C=C(B2OC(C)(C)C(C)(C)O2)C=C(N2C3C=CC=CC=3C3C=CC=CC2=3)C=1 |
| | (3-(carbazole-9H)Phenyl)Pinacol ester Usage And Synthesis |
| Uses | (3-(carbazole-9-yl)phenyl)pinacol boronic acid ester can be used as an intermediate in pharmaceutical and organic synthesis, and has a wide range of applications in laboratory research and development and chemical and pharmaceutical synthesis processes. | | Synthesis | Under nitrogen protection, 9-(3-bromophenyl)-9H-carbazole (10.5 g, 1.0 equiv), pinacol ester of bis(boronic acid) (9.93 g, 1.2 equiv), potassium acetate (10.9 g, 3.0 equiv), and anhydrous dimethylsulfoxide (190 mL) were added to the reaction vial, heated to 60 °C and stirred for 15 min. Subsequently, [1,1'-bis(diphenylphosphino)ferrocene]palladium(II) dichloride dichloromethane complex (0.799 g, 0.03 equiv) was added. The reaction mixture was heated to 80 °C and the reaction was continuously stirred for 9 hours. After completion of the reaction, it was cooled to room temperature. Water (250 mL) and toluene (500 mL) were added to the reaction solution and mixed with stirring. The aqueous layer was separated and the aqueous layer was extracted twice with toluene. The organic layers were combined and dried by adding magnesium sulfate and activated clay. The desiccant was removed by filtration and the toluene was removed by concentration under reduced pressure. The resulting solid was washed with cold methanol and dried under reduced pressure to give the target product 9-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-9H-carbazole (9.86 g, 80% yield) as white crystals. | | References | [1] Patent: EP1820801, 2007, A1. Location in patent: Page/Page column 83
[2] Patent: CN103951621, 2016, B. Location in patent: Paragraph 0072; 0073; 0074; 0077; 0078
[3] Patent: US2013/75706, 2013, A1. Location in patent: Paragraph 0075
[4] Patent: KR101622443, 2016, B1. Location in patent: Paragraph 0107; 0108; 0111; 0112
[5] Patent: US9379336, 2016, B2. Location in patent: Page/Page column 41; 42 |
| | (3-(carbazole-9H)Phenyl)Pinacol ester Preparation Products And Raw materials |
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