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4-Cyano-2-fluorobenzaldehyde

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4-Cyano-2-fluorobenzaldehyde manufacturers

4-Cyano-2-fluorobenzaldehyde Basic information
Product Name:4-Cyano-2-fluorobenzaldehyde
Synonyms:2-FLUORO-4-CYANOBENZALDEHYDE;Benzonitrile, 3-fluoro-4-formyl- (9CI);Benzonitrile, 3-fluoro-4-formyl-;3-Fluoro-4-formylbenzonitrile 99%;4-Cyano-2-fluorobenzaldehyde, 98%+;4-CYANO-2-FLUOROBENZALDEHYDE ISO 9001:2015 REACH;4-Cyano-2-fluorobenzaldehyde
CAS:105942-10-7
MF:C8H4FNO
MW:149.12
EINECS:
Product Categories:Fluorine series;HALIDE;ALDEHYDE;Drug Intermediates
Mol File:105942-10-7.mol
4-Cyano-2-fluorobenzaldehyde Structure
4-Cyano-2-fluorobenzaldehyde Chemical Properties
Melting point 73.2-75
Boiling point 275.8±25.0 °C(Predicted)
density 1.25±0.1 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
form crystalline solid
color Light brown
CAS DataBase Reference105942-10-7(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Hazard Note Irritant
HS Code 2926907090
MSDS Information
4-Cyano-2-fluorobenzaldehyde Usage And Synthesis
Synthesis
4-Bromo-3-fluorobenzonitrile

133059-44-6

TRIBUTYL(1-ETHOXYVINYL)TIN

97674-02-7

4-CYANO-2-FLUOROBENZALDEHYDE

105942-10-7

a) Preparation of the intermediate: 4-bromo-3-fluorobenzonitrile (6.0 g, 30.00 mmol) and tributyl(1-ethoxyvinyl)tin (11.2 mL, 33.00 mmol) were dissolved in toluene (100 mL) under nitrogen protection and stirred at room temperature. Dichlorobis(triphenylphosphine)palladium(II) (0.72 g, 1.03 mmol) was then added and stirring continued at room temperature. The reaction mixture was heated to reflux temperature and stirred overnight. After the reaction was completed, it was cooled to room temperature and 2 M potassium fluoride solution (50 mL) was slowly added and stirred for 30 minutes. Next, 6 M hydrochloric acid solution (100 mL) was added, heated to 70°C and stirred for 2 hours. The insoluble material was removed by filtration and the filtrate was extracted with ethyl acetate (3 × 80 mL). The organic layers were combined, washed with saturated brine, dried over anhydrous magnesium sulfate, filtered and the solvent was concentrated under reduced pressure. Intermediate 14 was obtained in a yield of 4.3 g, 88% yield.

References[1] Patent: WO2011/154298, 2011, A1. Location in patent: Page/Page column 36-37
Tag:4-Cyano-2-fluorobenzaldehyde(105942-10-7) Related Product Information
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