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6-CHLORO-2-PICOLINIC ACID METHYL ESTER

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6-CHLORO-2-PICOLINIC ACID METHYL ESTER Basic information

Product Name:
6-CHLORO-2-PICOLINIC ACID METHYL ESTER
Synonyms:
  • Methyl 6-Chloropyridine-2-carboxylate, 97+%
  • METHYL 6-CHLOROPYRIDINE-2-CARBOXYLATE
  • AKOS BBS-00004651
  • 6-CHLOROPYRIDINE-2-CARBOXYLIC ACID METHYL ESTER
  • 6-CHLORO-2-PICOLINIC ACID METHYL ESTER
  • 6-Chloro-2-pyridinecarboxylic acid methyl ester
  • 6-Chloropicolinic acid methyl ester
  • 2-Pyridinecarboxylic acid, 6-chloro-, methyl ester
CAS:
6636-55-1
MF:
C7H6ClNO2
MW:
171.58
EINECS:
808-173-1
Product Categories:
  • Picolinic acid series
Mol File:
6636-55-1.mol
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6-CHLORO-2-PICOLINIC ACID METHYL ESTER Chemical Properties

Melting point:
93-94°
Boiling point:
275.8±20.0 °C(Predicted)
Density 
1.294±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
pka
-1.03±0.10(Predicted)
form 
Solid
color 
Pale yellow
Water Solubility 
Slightly soluble in water.
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Safety Information

HazardClass 
IRRITANT
HS Code 
2933399990
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6-CHLORO-2-PICOLINIC ACID METHYL ESTER Usage And Synthesis

Uses

Methyl 6-chloropyridine-2-carboxylate was coupled with 2-(trimethylstannyl)pyridine to afford methyl 2,2?-bipyridine-6-carboxylate.

Synthesis Reference(s)

Synthetic Communications, 14, p. 77, 1984 DOI: 10.1080/00397918408060867

Synthesis

6-Chloro-2-picolinic acid methyl ester is prepared by the reaction of methanol and 6-Chloropicolinic acid. The specific synthesis steps are as follows:
Add thionyl chloride (3.7 ml, 50.8 mmol) to a solution of 6-chloropicolinic acid (4.0 g, 25.4 mmol) in methanol (85 ml) at 0 C. Stir the resultant solution for 15 minutes at 0 C, 0.5 hours at room temperature, and 6 hours at 50 C. Concentrate the reaction in vacuo and dilute with CHCl3 (150ml). Wash the organic solution with saturated aqueous sodium bicarbonate (3 x 100 ml), and brine (1 x 100 ml) and dry with sodium sulfate. Filtration and concentration afford methyl 6-chloropicolinate 4.38 g (100 percent) as a white solid. 1H NMR (CDCl3): δ 8.05 (m, 1H), 7.73 (m, 1H), 7.42 (m, 1H), 3.95 (s, 3H).

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