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(2-METHYL-PYRIDIN-3-YL)-METHANOL

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(2-METHYL-PYRIDIN-3-YL)-METHANOL Basic information

Product Name:
(2-METHYL-PYRIDIN-3-YL)-METHANOL
Synonyms:
  • 2-Methyl-3-hydroxyMethyl pyridine 97%
  • 3-Hydroxymethyl-2-methylpyridine (2-Methylpyridin-3-yl)methanol
  • 3-METHYL-3-HYDROXYMETHYL PYRIDINE
  • 3-(HYDROXYMETHYL)-ALPHA-PICOLINE
  • 3-Hydroxymethyl-2-methylpyridine
  • 3-Pyridinemethanol, 2-methyl-
  • (2-Mehtyl-pyridin-3-yl)-methanol
  • 2-Methyl-3-PyridineMethanol
CAS:
56826-61-0
MF:
C7H9NO
MW:
123.15
EINECS:
627-573-5
Mol File:
56826-61-0.mol
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(2-METHYL-PYRIDIN-3-YL)-METHANOL Chemical Properties

Boiling point:
262 °C (lit.)
Density 
1.106 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.545(lit.)
Flash point:
>230 °F
storage temp. 
Inert atmosphere,Room Temperature
Appearance
Light yellow to yellow Solid-liquid mixture
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HS Code 
2933399990

MSDS

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(2-METHYL-PYRIDIN-3-YL)-METHANOL Usage And Synthesis

Chemical Properties

light yellow oil liquid

Synthesis

65719-09-7

56826-61-0

A solution of methyl 2-methylnicotinate (35.2 g, 234 mmol) in 275 ml of dry ether was added dropwise to a vigorously stirred suspension of LiAlH4 (13.3 g, 350 mmol) in 600 ml of anhydrous ether. The reaction mixture was heated and refluxed in an oil bath at 55°C for 1.5 h and subsequently cooled to 0°C. H2O (64 ml) was added slowly dropwise, and the reaction was carried out for 1 h. The supernatant was decanted. The remaining suspension was extracted with ether. All organic phases were combined, dried over MgSO4 and the solvent was evaporated to give 29.9 g (234 mmol, 100% yield) of 3-(hydroxymethyl)-2-methylpyridine, the product being an orange-colored oil; GC analysis showed 100% purity.

References

[1] Patent: US2002/49316, 2002, A1
[2] Patent: US2005/124586, 2005, A1. Location in patent: Page/Page column 9-10
[3] Patent: WO2009/147211, 2009, A1. Location in patent: Page/Page column 25
[4] Patent: WO2009/42694, 2009, A1. Location in patent: Page/Page column 75
[5] Patent: US2004/6114, 2004, A1. Location in patent: Page 71

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