Simple exploration of C6H4Cl2N2O2

The synthetic route of 356783-14-7 has been constantly updated, and we look forward to future research findings.

Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. Generally, it requires fewer steps, and cheap raw materials. 356783-14-7, name is Methyl 3,6-dichloropyrazine-2-carboxylate, A new synthetic method of this compound is introduced below., COA of Formula: C6H4Cl2N2O2

REFERENTIAL EXAMPLE II-2 In 10 mL of methanol was dissolved 2.0 g of methyl 3,6-dichloro-2-pyrazinecarboxylate. Then, 10.2 mL of 1 mol/L aqueous solution of sodium hydroxide was added at an ice-cooled temperature and stirred at room temperature for one hour. The reaction mixture was poured into a mixture of 200 mL of ethyl acetate and 200 mL of water, and the organic layer was separated. The organic layer was washed successively with 50 mL of water and 50 mL of saturated aqueous solution of sodium chloride and dried on anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue thus obtained was washed with hexane to obtain 1.6 g of 3,6-dichloro-2-pyrazinecarboxylic acid as a white-colored solid product. R (KBr) cm-1: 1718 H-NMR (DMSO-d6) delta: 2.50(1H,s), 8.84(1H,s)

The synthetic route of 356783-14-7 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; Toyama Chemical Co., Ltd.; US2003/130213; (2003); A1;,
Pyrazine – Wikipedia,
Pyrazine | C4H4N2 – PubChem

Continuously updated synthesis method about 356783-14-7

According to the analysis of related databases, 356783-14-7, the application of this compound in the production field has become more and more popular.

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 356783-14-7 as follows. COA of Formula: C6H4Cl2N2O2

(a) In 20 mL of acetonitrile was dissolved 2.0 g of methyl 3,6-dichloro-2-pyrazinecarboxylate. After adding 2.8 g of potassium fluoride and 0.51 g of 18-crown-6-ether, the mixture thus obtained was heated under reflux for 9.5 hours in an atmosphere of nitrogen gas. After cooling, the solvent was removed under reduced pressure, and the residue was purified by silica gel chromatography [eluent: n-hexane:ethyl acetate=15:1] to obtain 1.1 g of methyl 3,6-difluoro-2-pyrazinecarboxylate as a colorless oily product. R (neat) cm-1: 1743 H-NMR (CDCl3) delta: 4.05(3H,s), 8.28(1H,dd,J=1.6 Hz, 8.4 Hz)

According to the analysis of related databases, 356783-14-7, the application of this compound in the production field has become more and more popular.

Reference:
Patent; Toyama Chemical Co., Ltd.; US2003/130213; (2003); A1;,
Pyrazine – Wikipedia,
Pyrazine | C4H4N2 – PubChem