Ethyl 2-chloro-6-methylpyridine-4-carboxylate, 97%
Ethyl 2-chloro-6-methylpyridine-4-carboxylate, 97% Basic information
- Product Name:
- Ethyl 2-chloro-6-methylpyridine-4-carboxylate, 97%
- Synonyms:
-
- Ethyl 2-chloro-6-methylpyridine-4-carboxylate, 97%
- 4-Pyridinecarboxylic acid, 2-chloro-6-Methyl-, ethyl ester
- 2-Chloro-6-methylpyridine-4-carboxylic acid ethyl ester
- JR-14076, Ethyl 2-chloro-6-methylpyridine-4-carboxylate, 97%
- 2-Chloro-6-methylisonicotinic Acid Ethyl Ester
- Ethyl 2-chloro-6-methyl-4-pyridinecarboxylate
- Ethyl 2-chloro-6-methylpyridine-4-carboxylate, 97%
- CAS:
- 3998-88-7
- MF:
- C9H10ClNO2
- MW:
- 199.63
- Mol File:
- 3998-88-7.mol
Ethyl 2-chloro-6-methylpyridine-4-carboxylate, 97% Chemical Properties
- Melting point:
- 65-67°C
- Boiling point:
- 107°C/1.5mm
- Density
- 1?+-.0.06 g/cm3(Predicted)
- Flash point:
- 107°C/1.5mm
- storage temp.
- Inert atmosphere,Room Temperature
- solubility
- soluble in Methanol
- form
- powder to crystal
- pka
- -0.14±0.10(Predicted)
- color
- White to Almost white
Ethyl 2-chloro-6-methylpyridine-4-carboxylate, 97% Usage And Synthesis
Synthesis
25462-85-5
64-17-5
3998-88-7
Step 1: Synthesis of ethyl 2-chloro-6-methylisonicotinate (97). Concentrated sulfuric acid (2 mL) was added dropwise to a stirred solution of 2-chloro-6-methylpyridine-4-carboxylic acid (7.0 g, 40.79 mmol) in ethanol (70 mL) at 0 °C. Subsequently, the reaction mixture was heated to 80 °C and kept for 12 hours. Upon completion of the reaction, the mixture was cooled to room temperature and concentrated under vacuum to remove the solvent. The concentrated residue was diluted with ethyl acetate and washed sequentially with water, sodium bicarbonate solution and saturated aqueous sodium chloride solution. The organic layer was separated, dried over anhydrous sodium sulfate, filtered and concentrated to give ethyl 2-chloro-6-methylisonicotinate (97) (7 g, 86% yield) as a white solid.
References
[1] Patent: US2010/249071, 2010, A1. Location in patent: Page/Page column 63-64
[2] Patent: WO2008/29371, 2008, A1. Location in patent: Page/Page column 41
[3] Patent: WO2009/24905, 2009, A1. Location in patent: Page/Page column 38-39; 49
[4] Patent: US2010/63108, 2010, A1. Location in patent: Page/Page column 16
[5] Patent: US2011/46170, 2011, A1. Location in patent: Page/Page column 17
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Ethyl 2-chloro-6-methylpyridine-4-carboxylate, 97%(3998-88-7)Related Product Information
- RARECHEM AL BW 1436
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- RARECHEM AL BW 2014