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| dibenzo[b,d]furan-3-ylboronic acid Basic information |
Product Name: | dibenzo[b,d]furan-3-ylboronic acid | Synonyms: | Boronic acid, 3-dibenzofuranyl-;Boronic acid,B-3-dibenzofuranyl-;dibenzo[b,d]furan-3-ylboronic acid;(3-Dibenzofuranyl)boronic acid;3-DBFBA;Dibenzo[b,d]furan-3-boronicacid;Dibenzofuran-3-ylboronic acid;Dibenzofuran-3-boronic acid | CAS: | 395087-89-5 | MF: | C12H9BO3 | MW: | 212.01 | EINECS: | | Product Categories: | OLED | Mol File: | 395087-89-5.mol | |
| dibenzo[b,d]furan-3-ylboronic acid Chemical Properties |
Boiling point | 438.5±37.0 °C(Predicted) | density | 1.34±0.1 g/cm3(Predicted) | storage temp. | under inert gas (nitrogen or Argon) at 2-8°C | pka | 8.20±0.30(Predicted) |
| dibenzo[b,d]furan-3-ylboronic acid Usage And Synthesis |
Uses | Dibenzo[b,d]furan-3-ylboronic acid can be used as organic synthesis intermediates and pharmaceutical intermediates, mainly used in laboratory research and development and chemical and pharmaceutical production processes. | Synthesis | In a 300 ml three-necked flask, 7.2 g of 4-bromodibenzofuran was dissolved in ?78° C. anhydrous tetrahydrofuran (THF) under an argon atmosphere. Then, 20 ml of an n-butyl lithium-n-hexane solution (1.6 M, 1.1 eq) was added and stirred for 1 hour. 4.23 ml (1.3 eq) of trimethoxyborane (B(OMe)3) was added and stirred for 2 hours, and the temperature of the reaction system was increased to room temperature. 200 ml of 1 N hydrochloric acid was added into the reactant and stirred for 3 hours. An organic layer was separated, and solvents were distilled off. In the crude product thus obtained, hexane was added. Precipitated product was filtered to obtain 4.94 g of dibenzofuran-4-boronic acid as a white solid (yield 80percent). The product was measured by FAB-MS, and dibenzofuran-4-boronic acid having a molecular weight of 212 was detected. |
| dibenzo[b,d]furan-3-ylboronic acid Preparation Products And Raw materials |
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