Basic information Safety Supplier Related

5-Methyl-1,3-thiazole-2-carboxaldehyde

Basic information Safety Supplier Related

5-Methyl-1,3-thiazole-2-carboxaldehyde Basic information

Product Name:
5-Methyl-1,3-thiazole-2-carboxaldehyde
Synonyms:
  • 5-Methylthiazole-2-carboxaldehyde
  • 2-Formyl-5-methyl-1,3-thiazole
  • 5-methyl-2-thiazolecarboxaldehyde
  • 5-Methyl-1,3-thiazole-2-carboxaldehyde
  • 5-methyl-1,3-thiazole-2-carbaldehyde
  • 2-Thiazolecarboxaldehyde, 5-methyl-
  • Methylthiazole-​
CAS:
13838-78-3
MF:
C5H5NOS
MW:
127.16
Product Categories:
  • Thiazoles, Isothiazoles & Benzothiazoles
  • Aldehydes
  • Thiazoles, Isothiazoles &Benzothiazoles
Mol File:
13838-78-3.mol
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5-Methyl-1,3-thiazole-2-carboxaldehyde Chemical Properties

Boiling point:
236.0℃
Density 
1.270
Flash point:
96.5℃
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
solid
pka
0.92±0.10(Predicted)
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Safety Information

HazardClass 
IRRITANT
HS Code 
2934100090
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5-Methyl-1,3-thiazole-2-carboxaldehyde Usage And Synthesis

Synthesis

3581-89-3

4394-85-8

13838-78-3

GENERAL STEPS: (a) Under argon protection, n-butyllithium (24 mL, 0.06 mol, 2.5 M hexane solution) was dissolved in 50 mL of ether and cooled to -78°C. Subsequently, a solution of 5-methylthiazole (5 g, 0.05 mol) dissolved in 25 mL of ether was added slowly and dropwise. The reaction mixture was stirred continuously at -78°C for 1 hour. Next, a solution of N-formylmorpholine (5.5 mL, 0.055 mol) dissolved in 30 mL of ether was added dropwise over 15 minutes. After addition, the mixture was continued to be stirred at -78°C for 1 hour, followed by warming to 0°-5°C and stirring overnight. Upon completion of the reaction, the reaction mixture was extracted with 4N HCl (4 x 10 mL), the aqueous phases were combined, cooled in an ice bath, and adjusted with sodium bicarbonate solution to pH 9. The aqueous phase was then extracted with ether (4 x 20 mL), the organic phases were combined, dried with magnesium sulfate, and concentrated under reduced pressure. The residue was dried under vacuum to give 4.5 g of 5-methyl-2-thiazolecarboxaldehyde in 70.8% yield.

References

[1] Patent: US5569655, 1996, A

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