[4-(trifluoromethyl)-1,3-thiazol-2-yl]methanol

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Products Intro: Product Name:(4-(Trifluoromethyl)thiazol-2-yl)methanol
CAS:204319-69-7
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CAS:204319-69-7
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CAS:204319-69-7
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Products Intro: Product Name:4-(trifluoromethyl)-1,3-thiazol-2-yl methanol
CAS:204319-69-7
Purity:97% Package:1G;5G;10g,25g,100g,500g
[4-(trifluoromethyl)-1,3-thiazol-2-yl]methanol Basic information
Product Name:[4-(trifluoromethyl)-1,3-thiazol-2-yl]methanol
Synonyms:[4-(trifluoromethyl)-1,3-thiazol-2-yl]methanol;(4-(Trifluoromethyl)thiazol-2-yl)methanol;2-Thiazolemethanol, 4-(trifluoromethyl)-
CAS:204319-69-7
MF:C5H4F3NOS
MW:183.15
EINECS:
Product Categories:
Mol File:204319-69-7.mol
[4-(trifluoromethyl)-1,3-thiazol-2-yl]methanol Structure
[4-(trifluoromethyl)-1,3-thiazol-2-yl]methanol Chemical Properties
Boiling point 205.1±40.0 °C(Predicted)
density 1.533±0.06 g/cm3(Predicted)
storage temp. 2-8°C
pka12.80±0.10(Predicted)
AppearanceWhite to off-white Solid
Safety Information
MSDS Information
[4-(trifluoromethyl)-1,3-thiazol-2-yl]methanol Usage And Synthesis
Synthesis
4-TRIFLUOROMETHYLTHIAZOLE-2-CARBOXYLIC ACID ETHYL ESTER

79247-86-2

[4-(trifluoromethyl)-1,3-thiazol-2-yl]methanol

204319-69-7

Sodium tetrahydroborate (840 mg) was slowly added to a methanolic solution (15 mL) of ethyl 4-trifluoromethylthiazole-2-carboxylate (2.5 g) at 0 °C, the reaction system was kept at 0 °C and stirred continuously for 2 hours. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure and the resulting residue was diluted with distilled water and subsequently extracted with ethyl acetate. The organic phases were combined, washed with saturated sodium chloride solution, dried over anhydrous magnesium sulfate and concentrated again under reduced pressure to remove the solvent. The final product was purified by silica gel column chromatography (NH silica gel, eluent hexane/ethyl acetate mixed solvent) to afford (4-(trifluoromethyl)thiazol-2-yl)methanol (1.7 g) as a white solid. The structure of the product was confirmed by 1H NMR (400 MHz, DMSO-d6): δ 4.78 (2H, d, J = 5.5 Hz), 6.28 (1H, t, J = 5.6 Hz), 8.41 (1H, s).

References[1] Patent: WO2015/5489, 2015, A1. Location in patent: Paragraph 0298
[2] Patent: WO2018/188795, 2018, A1. Location in patent: Page/Page column 51-52
[4-(trifluoromethyl)-1,3-thiazol-2-yl]methanol Preparation Products And Raw materials
Raw materials4-TRIFLUOROMETHYLTHIAZOLE-2-CARBOXYLIC ACID ETHYL ESTER
Preparation Productsmethyl({[4-(trifluoromethyl)-1,3-thiazol-2-yl]methyl})amine-->2-Thiazolecarboxaldehyde, 4-trifluoroMethyl-
Tag:[4-(trifluoromethyl)-1,3-thiazol-2-yl]methanol(204319-69-7) Related Product Information
4-TRIFLUOROMETHYLTHIAZOLE-2-CARBOXYLIC ACID ETHYL ESTER 2-Thiazolecarboxaldehyde, 4-trifluoroMethyl-