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79836-78-5

79836-78-5 Structure

79836-78-5 Structure
IdentificationBack Directory
[Name]

Ethyl 2-methylthiazole-5-carboxylate
[CAS]

79836-78-5
[Synonyms]

2-methyl-5-(carbethoxy)thiazole
ETHYL 2-METHYL-5-THIAZOLECARBOXYLATE
ETHYL 2-METHYL-THIAZOLE-5-CARBOXYLATE
5-(Ethoxycarbonyl)-2-methyl-1,3-thiazole
ETHYL2-METHYL-1,3-THIAZOLE-5-CARBOXYLATE
2-METHYL-THIAZOLE-5-CARBOXYLIC ACID ETHYL ESTER
5-Thiazolecarboxylicacid, 2-Methyl-, ethyl ester
[Molecular Formula]

C7H9NO2S
[MDL Number]

MFCD03840442
[MOL File]

79836-78-5.mol
[Molecular Weight]

171.22
Chemical PropertiesBack Directory
[Boiling point ]

117-120 °C
[density ]

1.198±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[form ]

solid
[pka]

1.61±0.10(Predicted)
[Appearance]

Colorless to yellow Liquid
[InChI]

1S/C7H9NO2S/c1-3-10-7(9)6-4-8-5(2)11-6/h4H,3H2,1-2H3
[InChIKey]

ORCQTMZHDQSNOJ-UHFFFAOYSA-N
[SMILES]

O=C(OCC)C1=CN=C(C)S1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
[WGK Germany ]

WGK 3
[HS Code ]

2934100090
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Synthesis Reference(s)]

Journal of the American Chemical Society, 104, p. 4461, 1982 DOI: 10.1021/ja00380a022
[Synthesis]

Thioacetamide

62-55-5

2-Chloro-3-oxopropionic acid ethyl ester

33142-21-1

Ethyl 2-methylthiazole-5-carboxylate

79836-78-5

To a stirred solution of ethyl 2-chloro-3-oxopropanoate (5.0 g, 33 mmol) in benzene (50 mL) under argon protection was added thioacetamide (2.5 g, 33 mmol) and the mixture was heated to reflux. After 4 h, the reaction mixture was cooled to room temperature, diluted with water (50 mL) and neutralized with saturated sodium bicarbonate solution to pH 7. Subsequently, the reaction mixture was extracted with ethyl acetate and the organic phases were combined and washed sequentially with water and brine. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated in vacuum. Purification by silica gel column chromatography (eluent: heptane/ethyl acetate, 0 to 50% gradient) afforded ethyl 2-methylthiazole-5-carboxylate (2.68 g, 47% yield) as a yellow liquid. Mass spectrometry (MS) analysis showed: m/e = 172.0 [M + H]+.

[References]

[1] Journal of the American Chemical Society, 1982, vol. 104, # 16, p. 4461 - 4465
[2] Patent: WO2010/127974, 2010, A1. Location in patent: Page/Page column 43
[3] Patent: WO2018/53157, 2018, A1. Location in patent: Page/Page column 108; 109
[4] Patent: WO2018/160878, 2018, A1. Location in patent: Page/Page column 278-279
[5] Journal of Chemical Research, 2011, vol. 35, # 5, p. 313 - 316
Spectrum DetailBack Directory
[Spectrum Detail]

Ethyl 2-methylthiazole-5-carboxylate(79836-78-5)1HNMR
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