Basic information Uses Safety Supplier Related

Oxazole-4-carbaldehyde

Basic information Uses Safety Supplier Related

Oxazole-4-carbaldehyde Basic information

Product Name:
Oxazole-4-carbaldehyde
Synonyms:
  • 1,3-oxazole-4-carbaldehyde
  • oxazol-4-carbaldehyde
  • 4-Oxazolecarboxaldehyde 97%
  • 4-FORMYLOXAZOLE
  • 4-OXAZOLECARBOXALDEHYDE
  • OXAZOLE-4-CARBALDEHYDE
  • 1,3-Oxazole-4-carboxaldehyde
  • 4-Formyl-1,3-oxazole
CAS:
118994-84-6
MF:
C4H3NO2
MW:
97.07
Product Categories:
  • Building Blocks
  • Oxazole
Mol File:
118994-84-6.mol
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Oxazole-4-carbaldehyde Chemical Properties

Melting point:
57-61 °C
Boiling point:
184.7±13.0 °C(Predicted)
Density 
1.258±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
solid
pka
-1.49±0.10(Predicted)
color 
Yellow
InChI
InChI=1S/C4H3NO2/c6-1-4-2-7-3-5-4/h1-3H
InChIKey
JBWIIXBEPINWPB-UHFFFAOYSA-N
SMILES
O1C=C(C=O)N=C1
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-36-43
Safety Statements 
26-36/37
WGK Germany 
3
HS Code 
2934999090
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Oxazole-4-carbaldehyde Usage And Synthesis

Uses

Oxazole-4-carboxaldehyde is mainly used in laboratory organic synthesis and in chemical and pharmaceutical research and development processes.

Synthesis

155742-48-6

118994-84-6

The general procedure for the synthesis of oxazole-4-carbaldehyde from 4-oxazolemethanol was as follows: a solution of anhydrous dichloromethane (200 mL) with dimethylsulfoxide (DMSO, 19.3 mL, 272 mmol) was added slowly and dropwise to a solution of anhydrous dichloromethane (200 mL) with oxalyl chloride (17.3 mL, 204 mmol) at -63 °C. The reaction mixture was stirred at -63 °C for 15 min before adding an anhydrous dichloromethane (200 mL) solution of 4-oxazole methanol (13.5 g, 204 mmol) with a controlled dropwise addition time of 15 min. Stirring was continued at -63 °C for 60 min, followed by the addition of triethylamine (Et3N, 53.1 mL, 381 mmol). The reaction mixture was gradually warmed up to room temperature. Upon completion of the reaction, the mixture was combined with 10% aqueous citric acid solution and extracted with dichloromethane (4 times) and ethyl acetate (2 times). The organic phases were combined, washed with a small amount of saturated aqueous sodium bicarbonate solution and extracted again with dichloromethane (3 times) and ethyl acetate (3 times). All organic phases were combined, dried with magnesium sulfate (MgSO4), filtered and the solvent was removed under reduced pressure. The residue was purified by column chromatography (eluent: ether/petroleum ether, ratio tapered from 1:1 to 2:1, to 4:1 and finally 1:0) to give oxazole-4-carbaldehyde (11.9 g, 86% yield). Thin layer chromatography (TLC) showed an Rf value of 0.65 (Expander: methanol/dichloromethane, 1:9).

References

[1] Patent: WO2006/21402, 2006, A1. Location in patent: Page/Page column 34
[2] Patent: WO2005/105802, 2005, A1. Location in patent: Page/Page column 109-110

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