Introduction of a new synthetic route about 651734-54-2

According to the analysis of related databases, 651734-54-2, the application of this compound in the production field has become more and more popular.

Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 651734-54-2, name is 2,6-Difluoro-3,5-dimethoxyaniline, This compound has unique chemical properties. The synthetic route is as follows., Application In Synthesis of 2,6-Difluoro-3,5-dimethoxyaniline

a) 5-[2,6-Difluoro-3,5-dimethoxy-phenylamino)-methyl]-2-methylsulfanyl-pyrimidin-4-ylamine A mixture of 4-Amino-2-methylsulfanyl-pyrimidine-5-carbaldehyde (2.45 g, 14.5 mmol), 2,6-difluoro-3,5-dimethoxyaniline (2.75 g, 14.5 mmol), and camphorsulfonic acid (1.01 g, 4.35 mmol) in toluene (80 ML) was heated at reflux for 18 hours (note: the flask was equipped with a Dean-Stark trap).The solvent was removed under reduced pressure to afford a yellow solid.The crude product was sufficiently pure, so it was taken on to the next step.To a suspension of the crude imine (~4.93 g) in tetrahydrofuran (60 ML) at 0 C., lithium aluminum hydride (820 mg, 21.6 mmol) was added in several portions.Caution, gas evolution! The resulting yellow suspension was then stirred at 0C. for 1 hour, whereupon a green solution was afforded.water (1 ML), 15% aqueous sodium hydroxide (1 ML), and water (3 ML) were added sequentially.Care is advised during this quenching protocol.The resulting mixture was then stirred at 0 C. for 10 minutes.The suspension was then filtered over a pad of Celite, and the Celite was rinsed with dichloromethane.The combined filtrates were concentrated under reduced to give a thick oil.Recrystallization was accomplished with a solvent mixture of dichloro-methane:hexanes:methanol (17:8.5:1, 312 ML) to give 1.85 g of the desired aniline.The mother liquor was concentrated and recrystallized with the same solvent mixture to give an additional 0.48 g of product.The second mother liquor was concentrated and recrystallized to afford 0.84 g.The precipitates were combined to give 3.17 g (64%, for 2 steps) of the title compound: MS (APCI) 343.1, 344.1.

According to the analysis of related databases, 651734-54-2, the application of this compound in the production field has become more and more popular.

Reference:
Patent; Chivikas Connolly, Cleo J.; Deur, Christopher James; Hamby, James Marino; Hoyer, Denton Wade; Limberakis, Chris; Reed, Jessica Elizabeth; Schroeder, Mel Conrad; Taylor, Clarke; US2004/19210; (2004); A1;,
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