ChemicalBook--->CAS DataBase List--->107512-35-6

107512-35-6

107512-35-6 Structure

107512-35-6 Structure
IdentificationBack Directory
[Name]

3,4-Dimethoxy-2-Methylpyridine
[CAS]

107512-35-6
[Synonyms]

Pantoprazole Impurity 38
3,4-Dimethoxy-2-Methylpyridine
Pyridine, 3,4-dimethoxy-2-methyl-
3,4-dimethoxy-2-methylpyridine (pantoprazole impurity)
[Molecular Formula]

C8H11NO2
[MDL Number]

MFCD16610899
[MOL File]

107512-35-6.mol
[Molecular Weight]

153.18
Chemical PropertiesBack Directory
[Boiling point ]

211.7±35.0 °C(Predicted)
[density ]

1.042±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

7.85±0.10(Predicted)
[Appearance]

Colorless to light yellow Liquid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

3,4-Dimethoxy-2-Methylpyridine(107512-35-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

3-HYDROXY-2-METHYL-4(1H)-PYRIDINONE

17184-19-9

Dimethyl sulfate

77-78-1

3,4-Dimethoxy-2-Methylpyridine

107512-35-6

General procedure: 38 g of 3-hydroxy-2-methylpyridin-4(1H)-one was added to a reaction flask and dissolved in a mixed solution of 90 g of water and 35 g of potassium hydroxide with stirring. The reaction temperature was controlled at 10~20°C. 75 g of dimethyl sulfate was slowly added dropwise, and the reaction was held at the same temperature for 20 hours after the dropwise addition. After completion of the reaction, 80 g of dichloromethane was added to the reaction mixture, stirred for 15 minutes and left to stratify. The aqueous layer was extracted once more with 20 g of dichloromethane, stirred for 15 minutes and left to stratify. The two dichloromethane layers were combined and concentrated under reduced pressure. The product was dried under reduced pressure to give 44 g of 3,4-dimethoxy-2-methylpyridine.

[References]

[1] Patent: CN104557692, 2018, B. Location in patent: Paragraph 0030; 0031
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