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1197-10-0

1197-10-0 Structure

1197-10-0 Structure
IdentificationBack Directory
[Name]

6-HYDROXYMETHYL-PYRIDINE-2-CARBOXYLIC ACID
[CAS]

1197-10-0
[Synonyms]

6-(Hydroxymethyl)picolinicaci
6-(hydroxymethyl)picolinic acid
6-HYDROXYMETHYL-PYRIDINE-2-CARBOXYLIC ACID
2-Pyridinecarboxylic acid, 6-(hydroxymethyl)-
6-(Hydroxymethyl)pyridine-2-carboxylic acid 95+%
2-Carboxy-6-(hydroxymethyl)pyridine, 6-(Hydroxymethyl)picolinic acid
[EINECS(EC#)]

200-258-5
[Molecular Formula]

C7H7NO3
[MDL Number]

MFCD09032021
[MOL File]

1197-10-0.mol
[Molecular Weight]

153.14
Chemical PropertiesBack Directory
[Melting point ]

137 °C
[Boiling point ]

381.2±32.0 °C(Predicted)
[density ]

1.404±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[pka]

0.96±0.50(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
[HazardClass ]

IRRITANT
Spectrum DetailBack Directory
[Spectrum Detail]

6-HYDROXYMETHYL-PYRIDINE-2-CARBOXYLIC ACID(1197-10-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

6-HYDROXYMETHYL-PYRIDINE-2-CARBOXYLIC ACID ETHYL ESTER

41337-81-9

6-HYDROXYMETHYL-PYRIDINE-2-CARBOXYLIC ACID

1197-10-0

General procedure for the synthesis of 6-carboxypyridine-2-methanol from ethyl 6-hydroxymethylpyridine-2-carboxylate: ethyl 6-hydroxymethylpyridine-2-carboxylate (200 mg, 1.1 mmol) was dissolved in methanol (1 mL). Subsequently, 2 N NaOH aqueous solution (1 mL) was added slowly and the reaction mixture was stirred at room temperature for 1 hour. Upon completion of the reaction, the reaction mixture was acidified to pH=3 with 2 N HCl. The solvent was removed by concentration under reduced pressure, and the residue was dissolved in methanol and filtered. The filtrate was concentrated under reduced pressure to give 6-carboxypyridine-2-methanol (150 mg, 89% yield, white solid).1H NMR (400 MHz, CD3OD) δ: 5.05 (s, 2H), 8.34 (d, J=8.0 Hz, 1H), 8.47 (d, J=8.0 Hz, 1H), 8.73 (d, J=8.0 Hz, 1H).

[References]

[1] Zeitschrift fuer Naturforschung, B: Chemical Sciences, 1994, vol. 49, # 8, p. 1127 - 1136
[2] Patent: WO2004/113281, 2004, A1. Location in patent: Page 57
[3] Journal of the American Chemical Society, 1982, vol. 104, # 8, p. 2251 - 2257
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