New learning discoveries about 109306-86-7

The chemical industry reduces the impact on the environment during synthesis 109306-86-7, I believe this compound will play a more active role in future production and life.

Application of 109306-86-7, With the rapid development and complex challenges of chemical substances, the synthesis of new drugs is usually one of the most effective ways to increase yield.109306-86-7, name is 2-(2-Bromophenyl)pyridine, molecular formula is C11H8BrN, molecular weight is 234.09, as common compound, the synthetic route is as follows.

Example 20The boronic acid compound D was synthesized as described below. That is, 2-(2-bromophenyl)pyridine (J. Am. Chem. Soc., 2006, vol. 128, p. 6,790 and 6,791.) (4.0 mmol) was added in a flask of 50 mL filled with dry nitrogen together with toluene (6.4 mL) and tetrahydrofuran (1.6 mL) as a solvent and was cooled to -78 C. After a 1.5-M hexane solution of butyl lithium (3.1 mL, 4.8 mmol) was added to this solution dropwise, and the mixture was stirred at -78 C. for 30 minutes. To the reaction mixture was added triisopropyl borate (4.8 mL), and the mixture was stirred at room temperature for 19 hours. After the reaction mixture was concentrated under reduced pressure, the residue was purified by column chromatography (alumina, ethyl acetate-methanol=5:1), so that methyl ester of the boronic acid compound D was obtained. After this product was dissolved in a mixture of water and methanol, the solvent was removed at 50 C. to 60 C. under reduced pressure, so that the boronic acid compound D was obtained (669 mg, yield: 84%). The structure of the boronic acid compound D was identified by 1H NMR and 13C NMR. 1H NMR (CD3OD) delta 7.42 (dt, J=1.5, 7.5 Hz, 1H), 7.47 (dt, J=1.5, 7.5 Hz, 1H), 7.60 (ddd, J=0.9, 1.5, 7.5 Hz, 1H), 7.64 (ddd, J=1.5, 5.7, 7.5 Hz, 1H), 7.96 (ddd, J=1.2, 1.5, 7.5 Hz, 1H), 8.18 (ddd, J=1.2, 1.5, 8.1 Hz, 1H), 8.27 (ddd, J=1.5, 7.5, 8.1 Hz, 1H), 8.49 (ddd, J=0.9, 1.5, 5.7 Hz, 1H); 13C NMR (CD3OD) delta 119.3, 123.2, 125.0, 129.5, 131.7, 132.3, 138.9, 143.1, 144.7, 157.1.

The chemical industry reduces the impact on the environment during synthesis 109306-86-7, I believe this compound will play a more active role in future production and life.

Reference:
Patent; NATIONAL UNIVERSITY CORPORATION NAGOYA UNIVERSITY; US2011/319620; (2011); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem