01/9/2021 News Simple exploration of 1033201-61-4

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,1033201-61-4, its application will become more common.

Electric Literature of 1033201-61-4, In the chemical reaction process,reaction time,type of solvent,can easily affect the result of the reaction, thereby determining the yield and properties of the reaction product.An updated downstream synthesis route of 1033201-61-4 as follows.

A slurry of 6-amino-3-bromopicolinic acid (25 g) in 400 mL 1:1 dichloromethane/chloroform was added to nitrosonium tetrafluoroborate (18.2 g) in dichloromethane (100 mL) at 5 C. over 1 hour. The resulting mixture was stirred for another 30 minutes, warmed to 35 C., and stirred overnight. The reaction mixture was cooled to room temperature and adjusted to pH 4 with a NaH2PO4 solution. The resulting solution was extracted three times with dichloromethane, and the combined extracts were washed with brine, dried over sodium sulfate, filtered and concentrated to provide the title compound.

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,1033201-61-4, its application will become more common.

Reference:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Sources of common compounds: 1033201-61-4

If you are interested in these compounds, you can also browse my other articles.Thank you for taking the time to read this article. I hope you enjoyed it, 1033201-61-4, 6-Amino-3-bromopicolinic acid.

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. 1033201-61-4, name is 6-Amino-3-bromopicolinic acid. This compound has unique chemical properties. The synthetic route is as follows. Safety of 6-Amino-3-bromopicolinic acid

A slurry of 6-amino-3-bromopicolinic acid (25 g) in 400 mL 1:1dichloromethane/chloroform was added to nitrosonium tetrafluoroborate (18.2 g) in dichloromethane(100 mL) at 5 oc over 1 hour. The resulting mixture was stirred for another 30 minutes, then warmed30 to 35 oc and stirred overnight. The reaction was cooled to room temperature, and then adjusted to pH4 with aqueous NaH2P04 solution. The resulting solution was extracted three times withdichloromethane, and the combined extracts were washed with brine, dried over sodium sulfate,filtered and concentrated to provide the title compound

If you are interested in these compounds, you can also browse my other articles.Thank you for taking the time to read this article. I hope you enjoyed it, 1033201-61-4, 6-Amino-3-bromopicolinic acid.

Reference:
Patent; ABBVIE INC.; BOGHAERT, Erwin, R.; SOUERS, Andrew, J.; PHILLIPS, Andrew, C.; JUDD, Andrew, S.; BRUNCKO, Milan; (717 pag.)WO2017/214282; (2017); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem