ChemicalBook--->CAS DataBase List--->869299-63-8

869299-63-8

869299-63-8 Structure

869299-63-8 Structure
IdentificationBack Directory
[Name]

3-ethyl-4-fluorobenzonitrile
[CAS]

869299-63-8
[Synonyms]

3-ethyl-4-fluorobenzonitrile
Benzonitrile, 3-ethyl-4-fluoro-
[Molecular Formula]

C9H8FN
[MDL Number]

MFCD19441199
[MOL File]

869299-63-8.mol
[Molecular Weight]

149.16
Chemical PropertiesBack Directory
[Boiling point ]

219.2±20.0 °C(Predicted)
[density ]

1.08±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2926907090
Spectrum DetailBack Directory
[Spectrum Detail]

3-ethyl-4-fluorobenzonitrile(869299-63-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

Diethylzinc

557-20-0

3-Bromo-4-fluorobenzonitrile

79630-23-2

3-ethyl-4-fluorobenzonitrile

869299-63-8

3-Bromo-4-fluorobenzonitrile (200 g, 1 mol) and [1,1'-bis(diphenylphosphino)ferrocene]palladium(II) dichloride dichloromethane complex (4.08 g, 5 mmol) were used as raw materials, which were dissolved in THF (1.2 L). A 1.0 M solution of diethylzinc hexane (600 mL, 0.6 mol) was slowly added at 40-50 °C, followed by heating the reaction mixture to 50-60 °C and maintaining the reaction for 4-5 hours. Complete reaction of the feedstock was confirmed by TLC monitoring. After completion of the reaction, the mixture was cooled to room temperature and quenched by addition of 5% dilute hydrochloric acid (1 L). The organic and aqueous layers were separated and the organic layer was washed twice with 500 mL of water followed by removal of solvent by concentration under reduced pressure. Hexane (600mL) and activated carbon (20g) were added to the concentrate and refluxed for 0.5 hours. After cooling to room temperature and filtration, activated carbon (10 g) was added to the filtrate and refluxing was repeated for 0.5 h. The filtrate was cooled and filtered. The filtrate was cooled to -50°C to -60°C and filtered to collect the solid. The resulting solid was dried under reduced pressure at 10-20 °C to give 3-ethyl-4-fluorobenzonitrile (112 g, 75% yield) as a white solid.

[References]

[1] Patent: CN108623496, 2018, A. Location in patent: Page/Page column 0049-0051; 0063-0065
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