ChemicalBook--->CAS DataBase List--->874822-98-7

874822-98-7

874822-98-7 Structure

874822-98-7 Structure
IdentificationBack Directory
[Name]

(5-Fluoro-2-methoxy-pyridin-3-yl)-methanol
[CAS]

874822-98-7
[Synonyms]

3-Pyridinemethanol, 5-fluoro-2-methoxy-
(5-Fluoro-2-methoxy-pyridin-3-yl)-methanol
[Molecular Formula]

C7H8FNO2
[MDL Number]

MFCD04972415
[MOL File]

874822-98-7.mol
[Molecular Weight]

157.14
Chemical PropertiesBack Directory
[Boiling point ]

236.2±35.0 °C(Predicted)
[density ]

1.260±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

12.80±0.10(Predicted)
[Appearance]

Off-white to light yellow Solid
Safety DataBack Directory
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

(5-Fluoro-2-methoxy-pyridin-3-yl)-methanol(874822-98-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methyl 5-fluoro-2-Methoxynicotinate

122433-52-7

(5-Fluoro-2-methoxy-pyridin-3-yl)-methanol

874822-98-7

General procedure for the synthesis of 5-fluoro-3-hydroxymethyl-2-methoxypyridine from 5-fluoro-2-methoxynicotinic acid methyl ester: To a 200 mL tetrahydrofuran solution of 5-fluoro-2-methoxynicotinic acid methyl ester (35, 10 g, 54.0 mmol) was added slowly and dropwise to lithium aluminum hydroxide (81 mL, 1 M solution in tetrahydrofuran, 81 mmol) at -78 °C. The reaction temperature was maintained at -78 °C and stirred for several hours. Upon completion of the reaction, 3 mL of water, 3 mL of 15% aqueous sodium hydroxide solution and 10 mL of water were added dropwise to quench the reaction. Subsequently, 200 mL of methyl tert-butyl ether was added for dilution. The solid insoluble material was removed by filtration and the filtrate was concentrated under vacuum to afford the target compound 5-fluoro-3-hydroxymethyl-2-methoxypyridine (36, 8 g, 50.9 mmol, 94% yield) as a white solid.

[References]

[1] Patent: US9096593, 2015, B2. Location in patent: Page/Page column 98; 99
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