ChemicalBook--->CAS DataBase List--->42508-74-7

42508-74-7

42508-74-7 Structure

42508-74-7 Structure
IdentificationBack Directory
[Name]

CHEMPACIFIC 38149
[CAS]

42508-74-7
[Synonyms]

CHEMPACIFIC 38149
(4-Methylpyridin-2-yl)
4-Methyl-2-PyridineMethanol
2-(Hydroxymethyl)-4-picoline
2-PyridineMethanol, 4-Methyl-
(4-METHYL-PYRIDIN-2-YL)-METHANOL
2-HYDROXYMETHYL-4-METHYL-PYRIDINE
[Molecular Formula]

C7H9NO
[MDL Number]

MFCD07774103
[MOL File]

42508-74-7.mol
[Molecular Weight]

123.15
Chemical PropertiesBack Directory
[Melting point ]

96℃
[Boiling point ]

236℃
[density ]

1.092
[Fp ]

96℃
[storage temp. ]

Inert atmosphere,Room Temperature
[pka]

13.50±0.10(Predicted)
[Appearance]

Colorless to light yellow Liquid
Spectrum DetailBack Directory
[Spectrum Detail]

CHEMPACIFIC 38149(42508-74-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

2,4-DIMETHYL-PYRIDINE 1-OXIDE

1122-45-8

CHEMPACIFIC 38149

42508-74-7

General procedure for the synthesis of (4-methyl-pyridin-2-yl)-methanol from 2,4-dimethylpyridine 1-oxide: to a solution of 2,4-dimethylpyridine 1-oxide (10.11 g, 82.10 mmol) in dichloromethane (DCM, 200 mL) was added slowly and dropwise Trifluoroacetic acid anhydride (TFAH, 51.37 g, 244.6 mmol) in a dichloromethane (DCM, 50 mL) solution. The reaction mixture was stirred at room temperature for 3.5 days. Upon completion of the reaction, the solvent was removed by concentration under reduced pressure. Methanol (MeOH, 200 mL) and saturated potassium carbonate (K2CO3, 250 mL) solution was then added and the mixture continued to be stirred for 3 hours at room temperature. Methanol was again removed by concentration under reduced pressure and the residue was extracted with dichloromethane (200 mL x 3). The organic phases were combined, dried over anhydrous sodium sulfate (Na2SO4), filtered and concentrated under reduced pressure to give 4 g of a brown oily product in 39.6% yield.

[References]

[1] Patent: CN106749268, 2017, A. Location in patent: Paragraph 0833; 0834
[2] Inorganic Chemistry, 2013, vol. 52, # 11, p. 6481 - 6501
[3] Pharmaceutical Bulletin, 1955, vol. 3, p. 413,415
[4] Yakugaku Zasshi, 1956, vol. 76, p. 900
[5] Chem.Abstr., 1957, p. 2770
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