2-Chloro-4,6-dimethyl-3-pyridinecarboxylic acid
2-Chloro-4,6-dimethyl-3-pyridinecarboxylic acid Basic information
- Product Name:
- 2-Chloro-4,6-dimethyl-3-pyridinecarboxylic acid
- Synonyms:
-
- 2-CHLORO-4,6-DIMETHYL-3-PYRIDINECARBOXYLIC ACID
- 2-chloro-4,6-dimethylpyridine-3-carboxylic acid
- 3-Pyridinecarboxylic acid, 2-chloro-4,6-dimethyl-
- 2-chloro-4,6-dimethylpyridine-3-carboxylicaci
- 2-Chloro-4,6-dimethyl-3-pyridinecarboxylic acid ISO 9001:2015 REACH
- CAS:
- 66662-48-4
- MF:
- C8H8ClNO2
- MW:
- 185.61
- Product Categories:
-
- Heterocycle
- Mol File:
- 66662-48-4.mol
2-Chloro-4,6-dimethyl-3-pyridinecarboxylic acid Chemical Properties
- Melting point:
- 139-140 °C(Solv: ethyl acetate (141-78-6))
- Boiling point:
- 342.3±37.0 °C(Predicted)
- Density
- 1.328±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 2.11±0.38(Predicted)
- Appearance
- White to off-white Solid
2-Chloro-4,6-dimethyl-3-pyridinecarboxylic acid Usage And Synthesis
Synthesis
14237-71-9
66662-48-4
Example C Synthesis of 2-chloro-4,6-dimethylnicotinic acid: 15 g of 2-chloro-3-cyano-4,6-dimethylpyridine [Jahine, J. prakt. Chem. 316, 337 (1974)] was mixed with 40 ml of concentrated sulphuric acid and 13 ml of fuming nitric acid, and heated with stirring to 95° C to initiate an exothermic reaction. The reaction temperature was maintained between 95 °C and 100 °C by cooling with ice water. After the exothermic reaction subsided, stirring was continued at 100°C for 30 minutes. Subsequently, the reaction mixture was decanted into ice and the pH was adjusted with ammonia to 3-4. The precipitate was collected by filtration and washed with water. The resulting solid was dehydrated by azeotropy with toluene in a device fitted with a water trap and finally recrystallized by toluene to give the target compound in 80% yield of the theoretical value with a melting point of 159-160°C. The results of elemental analysis were as follows: molecular formula C8H8ClNO2, molecular weight 185.6; calculated values: C 51.77%, H 4.34%, Cl 19.10%, N 7.55%; measured values: C 51.85%, H 4.36%, Cl 19.25%, N 7.56%.
References
[1] Patent: US4167570, 1979, A
[2] Chemistry of Heterocyclic Compounds, 2004, vol. 40, # 3, p. 308 - 314
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