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3-Pyridinemethanol,2-methoxy-(9CI)

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3-Pyridinemethanol,2-methoxy-(9CI) Basic information

Product Name:
3-Pyridinemethanol,2-methoxy-(9CI)
Synonyms:
  • (2-Methoxypyridin-3-yl)methanol 97%
  • 3-Pyridinemethanol,2-methoxy-(9CI)
  • (2-Methoxy-3-pyridinyl)methanol
  • (2-Methoxypyridin-3-yl)methanol
  • 3-Hydroxymethyl-2-methoxypyridine
  • 2-Methoxypyridine-3-methanol
  • (2-Methoxypyridin-3-yl)
  • 3-Pyridinemethanol, 2-methoxy-
CAS:
112197-16-7
MF:
C7H9NO2
MW:
139.15
Product Categories:
  • PYRIDINE
Mol File:
112197-16-7.mol
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3-Pyridinemethanol,2-methoxy-(9CI) Chemical Properties

Melting point:
lowmeltsolid°
Boiling point:
242℃
Density 
1.155
Flash point:
100℃
storage temp. 
Inert atmosphere,Room Temperature
pka
13.20±0.10(Predicted)
Appearance
White to off-white Solid
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Safety Information

RIDADR 
UN2811
HazardClass 
IRRITANT
HS Code 
2933399990
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3-Pyridinemethanol,2-methoxy-(9CI) Usage And Synthesis

Synthesis

67367-26-4

112197-16-7

General procedure for the synthesis of (2-methoxy-3-pyridine)methanol from methyl 2-methoxynicotinate: Example 138: Preparation of (2-methoxy-3-pyridine)methanol Methyl 2-methoxy-3-pyridinecarboxylate (1.021 g, 6.11 mmol) was dissolved in anhydrous tetrahydrofuran (5 mL) and lithium borohydride (0.266 g, 1.22 mmol) was added batchwise. The reaction mixture was heated to 70 °C and kept for 2 hours. Upon completion of the reaction, the reaction was quenched by the addition of saturated aqueous ammonium chloride, followed by three extractions with ethyl acetate (3×). The organic phases were combined, dried with magnesium sulfate and concentrated under reduced pressure to give (2-methoxy-3-pyridine)methanol as a colorless oil (0.849 g, 100% yield). 1H-NMR (400 MHz, CDCl3): δ 2.29 (1H, m, OH), 4.0 (3H, s, OCH3), 4.67 (2H, m, CH2), 6.89 (1H, m, Ar-H), 7.59 (1H, m, Ar-H), 8.1 (1H, m, Ar-H) ppm.

References

[1] Patent: WO2007/71900, 2007, A1. Location in patent: Page/Page column 95
[2] Synthetic Communications, 1996, vol. 26, # 12, p. 2257 - 2272
[3] Patent: US2007/49632, 2007, A1. Location in patent: Page/Page column 38
[4] Journal of Medicinal Chemistry, 2000, vol. 43, # 18, p. 3386 - 3399
[5] Patent: EP1422228, 2004, A1. Location in patent: Page 205-206

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