Introduction of a new synthetic route about 1462-37-9

The synthetic route of ((2-Bromoethoxy)methyl)benzene has been constantly updated, and we look forward to future research findings.

Electric Literature of 1462-37-9, In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. 1462-37-9, name is ((2-Bromoethoxy)methyl)benzene belongs to ethers-buliding-blocks compound, it is a common compound, a new synthetic route is introduced below.

To a solution of methyl 2-cyanoacetate (0.885 ml, 10.09 mmol) in DMF (20.18 ml) at rt was added sodium hydride (0.969 g, 24.22 mmol), and the reaction mixture was stirred at rt for 15 min. tetrabutylammonium iodide (0.373 g, 1.009 mmol) and ((2-bromoethoxy)methyl)benzene (3.35 ml, 21.19 mmol) were added, and the reaction mixture was stirred at 90 ¡ãC for 3 h. Water was added and the aqueous layer was extracted with ether (x3). The combined organic layers were washed with brine, dried over anhydrous sodium sulfate, and filtered, and the filltrate was evaporated in vacuo to give the crude product. The crude product was purified by silica gel chromatography eluting with 0-30percent ethyl acetate/hexanes to give methyl 4-(benzyloxy)-2-(2- (0187) (benzyloxy)ethyl)-2-cyanobutanoate (2.4 g, 6.53 mmol, 64.7 percent yield) as a colorless oil. NMR (500MHz, CHLOROFORM-d) delta 7.41 – 7.27 (m, 10H), 4.49 (s, 4H), 3.78 – 3.69 (m, 5H), 3.45 (s, 3H), 2.49 – 2.40 (m, 2H), 2.06 (dt, J=14.2, 4.7 Hz, 2H).

The synthetic route of ((2-Bromoethoxy)methyl)benzene has been constantly updated, and we look forward to future research findings.

Reference:
Patent; BRISTOL-MYERS SQUIBB COMPANY; WU, Yong-Jin; GUERNON, Jason M.; (102 pag.)WO2018/81384; (2018); A1;,
Ether – Wikipedia,
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