Identification | Back Directory | [Name]
4-Chloro-5-Methyl-2-pyridinecarboxylic acid | [CAS]
882679-14-3 | [Synonyms]
4-Chloro-5-methylpicolinic acid 4-Chloro-5-methylpyridine-2-carboxylic acid 4-Chloro-5-Methyl-2-pyridinecarboxylic acid 4-chloro-5-methyl-2-Pyridine carbocylic acid 2-Pyridinecarboxylic acid, 4-chloro-5-methyl- | [Molecular Formula]
C7H6ClNO2 | [MDL Number]
MFCD12400883 | [MOL File]
882679-14-3.mol | [Molecular Weight]
171.58 |
Chemical Properties | Back Directory | [Boiling point ]
332.5±37.0 °C(Predicted) | [density ]
1.390±0.06 g/cm3(Predicted) | [storage temp. ]
under inert gas (nitrogen or Argon) at 2-8°C | [pka]
3.44±0.10(Predicted) | [Appearance]
White to off-white Solid |
Hazard Information | Back Directory | [Synthesis]
General procedure for the synthesis of 4-chloro-5-methylpicolinic acid from ethyl 4-chloro-5-methylpyridine-2-carboxylate (CAS: 882679-12-1): ethyl 4-chloro-5-methylpyridine-2-carboxylate (10 g, 63 mmol) was dissolved in acetone (80 mL) at 0-5 °C, and potassium permanganate (13 g, 82 mmol) was slowly added to an aqueous solution (500 mL). The reaction mixture was heated to 55 °C and maintained for 1 hour. After completion of the reaction, the mixture was filtered through diatomaceous earth and the filtrate was concentrated under reduced pressure. The aqueous layer was acidified to pH 2-3 with an aqueous solution of 2 M hydrochloric acid.Subsequently, the mixture was extracted with a dichloromethane solution of 10% methanol (3 x 100 mL), the organic layers were combined, dried over anhydrous sodium sulfate, filtered and the solvent was evaporated in vacuum. The residue was crystallized by a solvent mixture of dichloromethane, ether and hexane to afford the target product 4-chloro-5-methylpicolinic acid (5 g, 46% yield). The product was analyzed by LC/MS with ESI m/z (M + H)+ = 172.2. | [References]
[1] Patent: WO2010/45188, 2010, A1. Location in patent: Page/Page column 73; 74 |
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Company Name: |
Cochemical Ltd.
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029-86115547 17791676824 |
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www.cochemical.com |
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