Basic information Safety Supplier Related

3-CHLORO-4-(TRIFLUOROMETHOXY)BENZALDEHYDE

Basic information Safety Supplier Related

3-CHLORO-4-(TRIFLUOROMETHOXY)BENZALDEHYDE Basic information

Product Name:
3-CHLORO-4-(TRIFLUOROMETHOXY)BENZALDEHYDE
Synonyms:
  • 3-CHLORO-4-(TRIFLUOROMETHOXY)BENZALDEHYDE
  • Benzaldehyde, 3-chloro-4-(trifluoromethyl)-
  • 3-chloro-4-trifluoromethoxybenaldehyde
CAS:
83279-38-3
MF:
C8H4ClF3O
MW:
208.57
Product Categories:
  • Fluorine series
  • Benzaldehyde
Mol File:
83279-38-3.mol
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3-CHLORO-4-(TRIFLUOROMETHOXY)BENZALDEHYDE Chemical Properties

Boiling point:
232.9±40.0 °C(Predicted)
Density 
1.42g/ml
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
liquid
color 
Clear, colourless
Water Solubility 
Insoluble in water.
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
Hazard Note 
Irritant
HS Code 
2913000090
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3-CHLORO-4-(TRIFLUOROMETHOXY)BENZALDEHYDE Usage And Synthesis

Uses

3-Chloro-4-(trifluoromethyl)benzaldehyde is used in synthesis of organic compunds in γ-Aminobutyrate-A Receptor Modulation by 3-Aryl-1-(arylsulfonyl)- 1,4,5,6-tetrahydropyridazines.

Synthesis

1092460-79-1

83279-38-3

The general procedure for the synthesis of 3-chloro-4-trifluoromethylbenzonitrile from 3-chloro-4-trifluoromethylbenzaldehyde was as follows: at 0 °C, using a syringe, diisobutylaluminum hydride (1.0 M toluene solution, 28 mL, 28 mmol) was added slowly and dropwise to 3-chloro-4-(trifluoromethyl)benzonitrile (3.79 g, 18.4 mmol) in tetrahydrofuran (THF, 50 mL ) solution. The reaction mixture was kept at 0 °C for 2 h, followed by warming to room temperature and continued stirring for 2 h. The reaction was carried out on a cooled surface. Upon completion of the reaction, the mixture was cooled to 0 °C and the reaction was quenched with 3M aqueous hydrochloric acid solution (75 mL). The mixture was warmed to room temperature and stirred vigorously for 1.5 hours. Subsequently, the mixture was transferred to a dispensing funnel and diluted with ether (Et2O). The organic phase was separated, dried over anhydrous sodium sulfate (Na2SO4), filtered and concentrated under reduced pressure. Purification by fast chromatography (Analogix? IntelliFlash 280? system, using 15% ethyl acetate/hexane as eluent, SF40-150g column) gave 2.84 g (74% yield) of 3-chloro-4-trifluoromethylbenzaldehyde as a colorless oil. The structure of the product was confirmed by 1H NMR (300 MHz, DMSO-d6): δ 10.09 (s, 1H), 8.21 (s, 1H), 8.12 (d, J = 8.1 Hz, 1H), 8.07-8.02 (m, 1H).

References

[1] Patent: US2009/124666, 2009, A1. Location in patent: Page/Page column 30-32

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