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| | 1,3,2-Dioxaborolane, 2,2'-(9,9-dimethyl-9H-fluorene-2,7-diyl)bis[4,4,5,5-tetramethyl] Basic information |
| Product Name: | 1,3,2-Dioxaborolane, 2,2'-(9,9-dimethyl-9H-fluorene-2,7-diyl)bis[4,4,5,5-tetramethyl] | | Synonyms: | 2,2'-(9,9-dimethyl-9H-fluorene-2,7-diyl);1,3,2-DIOXABOROLANE, 2,2''-(9,9-DIMETHYL-9H-FLUORENE-2,7-DIYL)BIS[4,4,5,5-TETRAMETHYL- (9CI);1,3,2-DIOXABOROLANE, 2,2'-(9,9-DIMETHYL-9H-FLUORENE-2,7-DIYL)BIS;9,9-DiMethylfluorene-2,7-diboronic acid bis(pinacol) ester, 95%;9,9-Dimethylfluorene-2,7-Bis(Boronic acid pinacol ester);2-[9,9-dimethyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-fluorenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;2-[9,9-dimethyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)fluoren-2-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;2,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9,9-dimethylfluorene | | CAS: | 325129-69-9 | | MF: | C27H36B2O4 | | MW: | 446.19 | | EINECS: | 805-553-9 | | Product Categories: | Boron Compounds | | Mol File: | 325129-69-9.mol | ![1,3,2-Dioxaborolane, 2,2'-(9,9-dimethyl-9H-fluorene-2,7-diyl)bis[4,4,5,5-tetramethyl] Structure](CAS/GIF/325129-69-9.gif) |
| | 1,3,2-Dioxaborolane, 2,2'-(9,9-dimethyl-9H-fluorene-2,7-diyl)bis[4,4,5,5-tetramethyl] Chemical Properties |
| Boiling point | 559.4±43.0 °C(Predicted) | | density | 1.09±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 | | CAS DataBase Reference | 325129-69-9 |
| | 1,3,2-Dioxaborolane, 2,2'-(9,9-dimethyl-9H-fluorene-2,7-diyl)bis[4,4,5,5-tetramethyl] Usage And Synthesis |
| Uses | 1,3,2-Dioxaborolane, 2,2''-(9,9-dimethyl-9h-fluorene-2,7-diyl)bis[4,4,5,5-tetramethyl] | | Synthesis | General procedure for the synthesis of 9,9-dimethylfluorene-2,7-diboronic acid pinacol ester from 2,7-dibromo-9,9-dimethylfluorene and pinacol ester of bis(pinacolato): 2,7-dibromo-9,9-dimethyl-9H-fluorene (130 g, 369 mmol), bis(pinacolato)diborane (225 g, 886 mmol), and potassium acetate (217 g, 2.22 mol ) were suspended in 1.4 L of dioxane. The mixed solution was degassed and saturated with argon. PdCl2(dppf)CH2Cl2 (15 g, 18 mmol) was subsequently added. The reaction mixture was heated to reflux and kept for 4 hours under the protection of inert atmosphere. After completion of the reaction, the mixture was filtered and the filtrate was washed with dioxane. The crude product was subjected to Soxhlet extraction using THF as a solvent to extract the residue, after which it was filtered again. A final 137 g of gray solid product was obtained in 83% of the theoretical yield. The purity of the product was confirmed by NMR (CDCl3 as solvent) and was greater than 95%. The following compounds were prepared using similar methods: | | References | [1] Patent: CN105636944, 2016, A. Location in patent: Paragraph 0213; 0214; 0215; 0216
[2] Patent: CN108558769, 2018, A. Location in patent: Paragraph 0068; 0069; 0071
[3] Journal of Medicinal Chemistry, 2014, vol. 57, # 5, p. 2033 - 2046
[4] Patent: WO2013/180376, 2013, A1. Location in patent: Paragraph 240; 241; 242; 243
[5] Patent: EP1762553, 2007, A1. Location in patent: Page/Page column 27-28 |
| | 1,3,2-Dioxaborolane, 2,2'-(9,9-dimethyl-9H-fluorene-2,7-diyl)bis[4,4,5,5-tetramethyl] Preparation Products And Raw materials |
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