Basic information Safety Supplier Related

4-(4-TRIFLUOROMETHYL-PHENOXY)-BENZALDEHYDE

Basic information Safety Supplier Related

4-(4-TRIFLUOROMETHYL-PHENOXY)-BENZALDEHYDE Basic information

Product Name:
4-(4-TRIFLUOROMETHYL-PHENOXY)-BENZALDEHYDE
Synonyms:
  • 4-(4-TRIFLUOROMETHYL-PHENOXY)-BENZALDEHYDE
  • Benzaldehyde, 4-[4-(trifluoromethyl)phenoxy]-
CAS:
90035-20-4
MF:
C14H9F3O2
MW:
266.22
Mol File:
90035-20-4.mol
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4-(4-TRIFLUOROMETHYL-PHENOXY)-BENZALDEHYDE Chemical Properties

Boiling point:
326.9±42.0 °C(Predicted)
Density 
1.297±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
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4-(4-TRIFLUOROMETHYL-PHENOXY)-BENZALDEHYDE Usage And Synthesis

Synthesis

402-45-9

459-57-4

90035-20-4

Intermediate 52: Synthesis of 4-{[4-(trifluoromethyl)phenyl]oxy}benzaldehyde; To a solution of 4-(trifluoromethyl)phenol (9.1 g, 56 mmol, 1.2 eq.) in N,N-dimethylformamide (DMF, 100 mL) was added sequentially cesium carbonate (22.8 g, 70 mmol, 1.5 eq.) and 4-fluorobenzaldehyde (5 mL, 46.6 mmol, 1.0 equiv). The reaction mixture was stirred and mixed at room temperature, then warmed to 85 °C and stirred continuously for 16 hours. After completion of the reaction, the mixture was cooled to room temperature and filtered to remove the insoluble salt. The filtrate was concentrated under reduced pressure to remove the solvent, and the crude product obtained was purified by fast column chromatography (silica gel, cyclohexane/ethyl acetate=70/30, v/v) to afford the target product 4-(4'-trifluoromethyl)phenoxybenzaldehyde (9.0 g, 73% yield) as a colorless oil. The structure of the product was confirmed by 1H NMR (CDCl3, δ 9.97 (s, 1H), 7.91 (m, 2H), 7.67 (d, J=8.6 Hz, 2H), 7.20-7.11 (m, 4H)) and LCMS ((M+H)+=267, retention time Rt=3.53 min).

References

[1] Patent: WO2010/15652, 2010, A2. Location in patent: Page/Page column 52-53
[2] Patent: WO2009/152082, 2009, A1. Location in patent: Page/Page column 59; 180
[3] Bioorganic and Medicinal Chemistry, 1998, vol. 6, # 1, p. 15 - 30
[4] Bioorganic and Medicinal Chemistry Letters, 2003, vol. 13, # 10, p. 1801 - 1804
[5] Journal of Medicinal Chemistry, 2015, vol. 58, # 7, p. 3036 - 3059

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