ChemicalBook--->CAS DataBase List--->13838-78-3

13838-78-3

13838-78-3 Structure

13838-78-3 Structure
IdentificationBack Directory
[Name]

5-Methyl-1,3-thiazole-2-carboxaldehyde
[CAS]

13838-78-3
[Synonyms]

2-Formyl-5-methyl-1,3-thiazole
5-methyl-2-thiazolecarboxaldehyde
5-Methylthiazole-2-carboxaldehyde
2-Thiazolecarboxaldehyde, 5-methyl-
5-methyl-1,3-thiazole-2-carbaldehyde
5-Methyl-1,3-thiazole-2-carboxaldehyde
[Molecular Formula]

C5H5NOS
[MDL Number]

MFCD08060733
[MOL File]

13838-78-3.mol
[Molecular Weight]

127.16
Chemical PropertiesBack Directory
[Boiling point ]

236.0℃
[density ]

1.270
[Fp ]

96.5℃
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[form ]

solid
[pka]

0.92±0.10(Predicted)
[InChI]

1S/C5H5NOS/c1-4-2-6-5(3-7)8-4/h2-3H,1H3
[InChIKey]

UUIAJFQYWAFZEO-UHFFFAOYSA-N
[SMILES]

Cc1cnc(C=O)s1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H317-H319
[Precautionary statements ]

P280-P305+P351+P338
[WGK Germany ]

WGK 3
[HazardClass ]

IRRITANT
[HS Code ]

2934100090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Eye Irrit. 2
Spectrum DetailBack Directory
[Spectrum Detail]

5-Methyl-1,3-thiazole-2-carboxaldehyde(13838-78-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

5-Methylthiazole

3581-89-3

4-Formylmorpholine

4394-85-8

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

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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