Basic information Safety Supplier Related

4-(2-PHENYLETH-1-YNYL)BENZALDEHYDE

Basic information Safety Supplier Related

4-(2-PHENYLETH-1-YNYL)BENZALDEHYDE Basic information

Product Name:
4-(2-PHENYLETH-1-YNYL)BENZALDEHYDE
Synonyms:
  • 4-PHENYLETHYNYL-BENZALDEHYDE
  • BUTTPARK 46\04-33
  • 4-(2-PHENYLETH-1-YNYL)BENZALDEHYDE
  • 4-(2-phenylethynyl)benzaldehyde
  • 4-Phenylethynyl-benzaldehyd
  • Benzaldehyde, 4-(2-phenylethynyl)-
  • Product English Name: 4-(Phenylethynyl)benzaldehyde
CAS:
57341-98-7
MF:
C15H10O
MW:
206.24
Product Categories:
  • Aldehydes
  • Phenyls & Phenyl-Het
  • Phenyls & Phenyl-Het
Mol File:
57341-98-7.mol
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4-(2-PHENYLETH-1-YNYL)BENZALDEHYDE Chemical Properties

Melting point:
102 °C
Boiling point:
364.2±25.0 °C(Predicted)
Density 
1.14±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
crystalline solid
color 
Light yellow
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Safety Information

Hazard Codes 
Xi
HazardClass 
IRRITANT
HS Code 
2912290090
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4-(2-PHENYLETH-1-YNYL)BENZALDEHYDE Usage And Synthesis

Synthesis

87199-17-5

536-74-3

57341-98-7

4-Formylphenylboronic acid (0.5 mmol), phenylacetylene (0.6 mmol), dichloromethane (2 mL), Catalyst 3 (2 mol%), silver oxide (Ag2O, 1.0 mmol), and potassium acetate (KOAc, 1.0 mmol) were sequentially added to the Schlenk tube. The reaction mixture was stirred at 35 °C for 24 h under argon protection. Upon completion of the reaction, excess dichloromethane was removed by rotary evaporation and the residue was purified directly by silica gel column chromatography (eluent was petroleum ether or mixed petroleum ether/ethyl acetate solvent) to afford the target product, 4-(phenylalkynyl)benzaldehyde (32d, Table 1, entry 11) (99 mg, 96% yield). The product was a white solid, melting point: 98-100 °C; 1H NMR (400 MHz, CDCl3) δ 9.99 (s, 1H), 7.84 (d, J = 7.8 Hz, 2H), 7.66 (d, J = 8.0 Hz, 2H), 7.56 (dd, J = 3.4, 2.9 Hz, 2H), 7.37 (s, 3H); 13C NMR ( 100 MHz, CDCl3) δ 191.6, 135.3, 132.0, 131.7, 129.6, 128.9, 128.43, 128.41, 122.4, 93.5, 88.5.

References

[1] Tetrahedron, 2014, vol. 70, # 35, p. 5980 - 5985
[2] Transition Metal Chemistry, 2017, vol. 42, # 7, p. 579 - 585
[3] Catalysis Science and Technology, 2014, vol. 4, # 5, p. 1276 - 1285

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