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(6-Chloro-2-pyridinyl)methanol

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(6-Chloro-2-pyridinyl)methanol Basic information

Product Name:
(6-Chloro-2-pyridinyl)methanol
Synonyms:
  • CHEMPACIFIC 38159
  • (6-CHLORO-PYRIDIN-2-YL)-METHANOL
  • (6-Chloro-2-pyridinyl)methanol
  • 2-Chloro-6-(Hydroxymethyl)Pyridine
  • 6-Chloro-2-pyridinemethanol
  • 2-Chloropyridine-6-Methanol
  • 2-Pyridinemethanol, 6-chloro-
  • (6-Chloro-2-pyridinyl)methanol ISO 9001:2015 REACH
CAS:
33674-97-4
MF:
C6H6ClNO
MW:
143.57
EINECS:
807-010-1
Mol File:
33674-97-4.mol
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(6-Chloro-2-pyridinyl)methanol Chemical Properties

Boiling point:
251.8±25.0 °C(Predicted)
Density 
1.324±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
13.12±0.10(Predicted)
form 
liquid
color 
Colourless
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Safety Information

HazardClass 
IRRITANT
HS Code 
2933399990
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(6-Chloro-2-pyridinyl)methanol Usage And Synthesis

Synthesis

6636-55-1

33674-97-4

General procedure for the synthesis of 2-chloro-6-hydroxymethylpyridine from methyl 6-chloropyridine-2-carboxylate: 6.7 g (39.0 mmol) of methyl 6-chloropyridine-2-carboxylate was dissolved in 90 mL of anhydrous tetrahydrofuran, which was subsequently cooled to -45 °C. A 40 mL solution of 1 M lithium aluminum hydride in tetrahydrofuran was added slowly and dropwise over 30 min. The reaction mixture was stirred at -45°C for 30 minutes and then slowly warmed to 0°C and continued stirring for 30 minutes. Subsequently, 15 mL of 1 N aqueous sodium hydroxide solution was slowly added dropwise to quench the reaction. Solid impurities were removed by diatomaceous earth filtration and the filtrate was concentrated to give 5.08 g (35.4 mmol, 91% yield) of 2-chloro-6-hydroxymethylpyridine. The product was characterized by 1H NMR (CDCl3, ppm): δ 7.61 (1H, d), 7.30 (1H, t), 7.04 (1H, d), 3.72 (2H, s).FAB MS (m/z) = 144 [M + 1].

References

[1] Patent: WO2007/58482, 2007, A1. Location in patent: Page/Page column 47-48

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