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| | 4-Fluoro-2-methylphenylboronic acid Basic information |
| | 4-Fluoro-2-methylphenylboronic acid Chemical Properties |
| Melting point | 191-196 °C(lit.) | | Boiling point | 277.4±50.0 °C(Predicted) | | density | 1.20±0.1 g/cm3(Predicted) | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | solubility | Chloroform (Slightly, Sonicated), DMSO (Slightly), Methanol (Slightly) | | form | Powder | | pka | 8.75±0.58(Predicted) | | color | White to off-white | | InChI | InChI=1S/C7H8BFO2/c1-5-4-6(9)2-3-7(5)8(10)11/h2-4,10-11H,1H3 | | InChIKey | IQMLIVUHMSIOQP-UHFFFAOYSA-N | | SMILES | B(C1=CC=C(F)C=C1C)(O)O | | CAS DataBase Reference | 139911-29-8(CAS DataBase Reference) |
| | 4-Fluoro-2-methylphenylboronic acid Usage And Synthesis |
| Chemical Properties | white to off-white powder | | Uses | suzuki reaction | | Synthesis | The general procedure for the synthesis of 4-fluoro-2-methylphenylboronic acid from triisopropyl borate and 2-bromo-5-fluorotoluene was carried out as follows: 2-bromo-5-fluorotoluene (250 g) was dissolved in a solvent mixture of tetrahydrofuran (250 ml) and n-hexane (250 ml) under dry conditions, and cooled to -78 °C. At this temperature, n-butyllithium (991.5 ml) was slowly added dropwise and the reaction temperature was maintained in an ice bath. After the dropwise addition, the reaction mixture was stirred for 1 hour. Subsequently, triisopropyl borate (373.11 g) was added dropwise and stirring was continued at -78°C for 1 hour. After completion of the reaction, the reaction mixture was diluted with aqueous sodium hydroxide solution and then washed with n-heptane. The pH of the aqueous layer was adjusted to 2-3 with hydrochloric acid followed by extraction with ethyl acetate. The organic layers were combined and concentrated under vacuum. The concentrated product was dissolved in ethyl acetate at about 40 °C and n-heptane was added to promote crystallization, resulting in 4-fluoro-2-methylphenylboronic acid. The yield was 61.5% and the HPLC purity was 99.00%. | | References | [1] Patent: WO2017/125835, 2017, A1. Location in patent: Paragraph 00117 |
| | 4-Fluoro-2-methylphenylboronic acid Preparation Products And Raw materials |
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