Basic information Safety Supplier Related

3-Methoxy-4-(4-methyl-1H-imidazol-1-yl)benzaldehyde

Basic information Safety Supplier Related

3-Methoxy-4-(4-methyl-1H-imidazol-1-yl)benzaldehyde Basic information

Product Name:
3-Methoxy-4-(4-methyl-1H-imidazol-1-yl)benzaldehyde
Synonyms:
  • 3-methoxy-4-(4-methylimidazole)benzaldehyd
  • 3-METHOXY-4-(4-METHYL-1H-IMIDAZOL-1-YL)BENZALDEHYDE
  • 3-METHOXY-4-(4-METHYL-IMIDAZOL-1-YL)-BENZALDEHYDE
  • Benzaldehyde, 3-methoxy-4-(4-methyl-1H-imidazol-1-yl)-
  • 3-Methoxy-4-(4-methyl-1H-imidazol-1-yl)
  • 3-methoxy-4-(4-methyl-1-imidazolyl)benzaldehyde
  • 3-Methoxy-4-(4-methyl-imidazol-1-yl)-benzaldehyde, CAS 870837-18-6
CAS:
870837-18-6
MF:
C12H12N2O2
MW:
216.24
Mol File:
870837-18-6.mol
More
Less

3-Methoxy-4-(4-methyl-1H-imidazol-1-yl)benzaldehyde Chemical Properties

Boiling point:
415.1±40.0 °C(Predicted)
Density 
1.16
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
5.43±0.61(Predicted)
Appearance
Light yellow to yellow Solid
More
Less

3-Methoxy-4-(4-methyl-1H-imidazol-1-yl)benzaldehyde Usage And Synthesis

Synthesis

822-36-6

128495-46-5

870837-18-6

General procedure for the synthesis of 3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzaldehyde from 4-methylimidazole and 3-methoxy-4-fluorobenzaldehyde: 4-fluoro-3-methoxybenzaldehyde (85 g, 0.55 mol), 4-methyl-1H-imidazole (90.5 g, 1.1 mol) and cesium carbonate (268.8 g, 0.82 mol) were mixed in dimethylformamide (1.7 L) were mixed and the reaction was stirred at 100 °C for 1 hour. After completion of the reaction, the mixture was cooled to room temperature, filtered, and the filtrate was concentrated under reduced pressure. The concentrated residue was dissolved in water (2 L) and extracted with ethyl acetate (3 x 2 L). The organic layers were combined, washed sequentially with water and brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to remove the solvent. Purification by silica gel column chromatography (eluent ratio petroleum ether:ethyl acetate = 2:1) gave a yellow solid. The solid was recrystallized with ethyl acetate (300 mL) to give 3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzaldehyde in white solid form. Yield: 17.8 g, 0.082 mol, 15% yield.1H NMR (300 MHz, CDCl3) δ 2.31 (d, J = 1.0 Hz, 3H), 3.97 (s, 3H), 7.01 (m, 1H), 7.45 (d, J = 7.8 Hz, 1H), 7.54-7.58 (m, 2H), 7.83 (d, J = 1.3 Hz, 1H), 10.01 (s, 1H).

References

[1] Patent: WO2010/100606, 2010, A1. Location in patent: Page/Page column 41-42
[2] Bioorganic and Medicinal Chemistry Letters, 2011, vol. 21, # 2, p. 773 - 776
[3] Bioorganic and Medicinal Chemistry Letters, 2011, vol. 21, # 13, p. 4083 - 4087
[4] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 9, p. 3140 - 3146
[5] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 9, p. 3140 - 3146

3-Methoxy-4-(4-methyl-1H-imidazol-1-yl)benzaldehydeSupplier

Shanghai Ennopharm Co., Ltd.
Tel
+86 (21) 6435-5022
China Langchem Inc.
Tel
0086-21-58956006
T&W GROUP
Tel
021-61551611 13296011611
Email
contact@trustwe.com
Shanghai T&W Pharmaceutical Co., Ltd.
Tel
+86 21 61551611
Shanghai Raise Chemical Technology Co.,Ltd
Tel
15026594951
Email
rs@raise-chem.com