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ChemicalBook--->CAS DataBase List--->884494-81-9

884494-81-9

884494-81-9 Structure

884494-81-9 Structure
IdentificationBack Directory
[Name]

3-BROMO-5-FLUORO-2-METHOXYPYRIDINE
[CAS]

884494-81-9
[Synonyms]

uoro-2-methoxypyridine
3-BROMO-5-FLUORO-2-METHOXYPYRIDINE
Pyridine, 3-bromo-5-fluoro-2-methoxy-
3-Bromo-5-fluoro-2-methoxypyridine 98%
3-Bromo-5-fluoro-2-methoxypyridine ,98%
3-Bromo-5-fluoropyridin-2-yl methyl ether
3-BROMO-5-FLUORO-2-METHOXYPYRIDINE ISO 9001:2015 REACH
[Molecular Formula]

C6H5BrFNO
[MDL Number]

MFCD04972397
[MOL File]

884494-81-9.mol
[Molecular Weight]

206.01
Chemical PropertiesBack Directory
[Boiling point ]

188.4±35.0 °C(Predicted)
[density ]

1.621±0.06 g/cm3(Predicted)
[refractive index ]

1.5390 to 1.5430
[storage temp. ]

Inert atmosphere,2-8°C
[form ]

Liquid
[pka]

-1.38±0.20(Predicted)
[Appearance]

Colorless to light yellow Solid-Liquid Mixture
[Sensitive ]

Light Sensitive
[CAS DataBase Reference]

884494-81-9
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H312-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P304+P340-P305+P351+P338-P405-P501a
[HS Code ]

2933399990
Hazard InformationBack Directory
[Uses]

3-Bromo-5-fluoro-2-methoxypyridine is a compound used in the synthesis of 5-Fluoro-2-methoxy-3-(2R)-2-pyrrolidinylpyridine (1213093-30-1).
[Synthesis]

2-BROMO-5-FLUORO-2-HYDROXYPYRIDINE

884494-94-4

Iodomethane

74-88-4

3-Bromo-5-fluoro-2-methoxypyrdine

884494-81-9

General steps: 1. Prepare raw material: (R)-5-fluoro-2-methoxy-3-(pyrrolidin-2-yl)pyridine. 2. Step A: Synthesis of 3-bromo-5-fluoro-2-methoxypyridine. a. Add 3-bromo-5-fluoropyridin-2(1H)-one (10.0 g, 52.1 mmol) and Ag2CO3 (10.0 g, 36.5 mmol) to toluene (100 mL). b. Slowly add iodomethane (3.89 mL, 62.5 mmol). c. The reaction mixture was stirred at room temperature overnight. d. Upon completion of the reaction, filter through diatomaceous earth and wash the solids with toluene. e. The filtrate was concentrated to give the crude product. f. The crude product was purified by silica gel column chromatography (eluent: 5-25% EtOAc/hexane) to afford 3-bromo-5-fluoro-2-methoxypyridine (4.70 g, 43.8% yield) as a colorless oil.

[References]

[1] Patent: WO2011/6074, 2011, A1. Location in patent: Page/Page column 74-75
Spectrum DetailBack Directory
[Spectrum Detail]

3-Bromo-5-fluoro-2-methoxypyrdine(884494-81-9)1HNMR
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