Analyzing the synthesis route of 2,3,6-Trichloropyridine

According to the analysis of related databases, 6515-09-9, the application of this compound in the production field has become more and more popular.

Related Products of 6515-09-9, Adding some certain compound to certain chemical reactions, such as: 6515-09-9, name is 2,3,6-Trichloropyridine,molecular formula is C5H2Cl3N, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound 6515-09-9.

EXAMPLE 2 Preparation of 3,6-dichloro-2-(dichloromethyl)pyridine (Cpd. 2 of table) STR4 2,3,6-Trichloropyridine (1.0 g, 0.0055 mole) was combined with 4 g N-methylpyrrolidone, 4 g (0.033 mole) of chloroform, and 1.0 g of 50 percent aqueous sodium hydroxide (0.013 mole). The resulting mixture was stirred and warmed mildly for about 1 hour at which time the product was found to be present in the reaction mixture by gas chromatography and mass spectrometry using an authentic sample of the product as a standard. After standing overnight at ambient temperature the title compound represented about 1.7 percent of the pyridines in the mixture.

According to the analysis of related databases, 6515-09-9, the application of this compound in the production field has become more and more popular.

Reference:
Patent; The Dow Chemical Company; US4739070; (1988); A;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem