ChemicalBook--->CAS DataBase List--->894779-76-1

894779-76-1

894779-76-1 Structure

894779-76-1 Structure
IdentificationBack Directory
[Name]

2-Cyano-5-fluorobenzaldehyde
[CAS]

894779-76-1
[Synonyms]

2-Cyano-5-fluorobenzaldehyde
4-Fluoro-2-forMylbenzonitrile
Benzonitrile, 4-fluoro-2-formyl-
2-Cyano-5-fluorobenzaldehyde ISO 9001:2015 REACH
[Molecular Formula]

C8H4FNO
[MDL Number]

MFCD16619724
[MOL File]

894779-76-1.mol
[Molecular Weight]

149.12
Chemical PropertiesBack Directory
[Boiling point ]

288.0±25.0 °C(Predicted)
[density ]

1.25±0.1 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[Appearance]

Light yellow to light brown Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2926907090
Spectrum DetailBack Directory
[Spectrum Detail]

2-Cyano-5-fluorobenzaldehyde(894779-76-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-Bromo-4-fluorobenzonitrile

36282-26-5

N,N-Dimethylformamide

68-12-2

2-Cyano-5-fluorobenzaldehyde

894779-76-1

To an anhydrous tetrahydrofuran (THF, 20 mL) solution of 2-bromo-4-fluorobenzonitrile (5.0 g, 25.0 mmol) was slowly added isopropylmagnesium chloride (PrMgCl, 2.0 M solution of THF, 15.0 mL, 30.0 mmol) at -30 °C. The reaction temperature was maintained at -30°C with continuous stirring for 3 hours. Subsequently, N,N-dimethylformamide (DMF, 5.80 mL, 75.0 mmol) was added to the reaction system. The reaction mixture was gradually warmed to room temperature and stirring was continued for 1 hour. Upon completion of the reaction, the mixture was cooled to -10 °C, 2 M hydrochloric acid (37 mL) was slowly added and stirred at this temperature for 20 min. The reaction solution was concentrated in vacuum to 1/3 of the original volume and then extracted with ethyl acetate (EtOAc, 3 times). The organic phases were combined, dried with anhydrous sodium sulfate (Na2SO4), filtered and concentrated to give the target product 4-fluoro-2-formylbenzonitrile (3.9 g, 71% yield).

[References]

[1] Patent: WO2011/68821, 2011, A1. Location in patent: Page/Page column 137
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