4-(TrifluoroMethoxy)benzeneacetic acid ethyl ester

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Products Intro: Product Name:Ethyl 2-(4-(trifluoromethoxy)phenyl)acetate
CAS:1206550-93-7
Purity:98% Package:1kg,5kg,10kg
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Products Intro: Product Name:(4-TRIFLUOROMETHOXY-PHENYL)-ACETIC ACID ETHYL ESTER
CAS:1206550-93-7
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Products Intro: Product Name:Ethyl 2-(4-(trifluoromethoxy)phenyl)acetate
CAS:1206550-93-7
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Products Intro: Product Name:4-(Trifluoromethoxy)benzeneacetic acid ethyl ester
CAS:1206550-93-7
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Products Intro: Product Name:4-(TrifluoroMethoxy)benzeneacetic acid ethyl ester
CAS:1206550-93-7
Purity:98% Package:5KG;1KG
4-(TrifluoroMethoxy)benzeneacetic acid ethyl ester Basic information
Product Name:4-(TrifluoroMethoxy)benzeneacetic acid ethyl ester
Synonyms:4-(TrifluoroMethoxy)benzeneacetic acid ethyl ester;(4-Trifluoromethoxy-phenyl)-acetic acid ethyl ester;ethyl 2-(4-(trifluoromethoxy)phenyl)acetate;Ethyl 2-(4-(trifluoromethoxy);Benzeneacetic acid, 4-(trifluoromethoxy)-, ethyl ester
CAS:1206550-93-7
MF:C11H11F3O3
MW:248.2
EINECS:
Product Categories:
Mol File:1206550-93-7.mol
4-(TrifluoroMethoxy)benzeneacetic acid ethyl ester Structure
4-(TrifluoroMethoxy)benzeneacetic acid ethyl ester Chemical Properties
Boiling point 240.6±35.0 °C(Predicted)
density 1.246±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
AppearanceColorless to off-white Solid-Liquid Mixture
Safety Information
MSDS Information
4-(TrifluoroMethoxy)benzeneacetic acid ethyl ester Usage And Synthesis
Chemical Propertieslight yellow liquid
Synthesis
Ethanol

64-17-5

4-(TRIFLUOROMETHOXY)PHENYLACETIC ACID

4315-07-5

4-(TrifluoroMethoxy)benzeneacetic acid ethyl ester

1206550-93-7

a) Concentrated sulfuric acid (0.484 mL, 9.08 mmol) was added slowly and dropwise to a solution of 2-(4-(trifluoromethoxy)phenyl)acetic acid (2.0 g, 9.08 mmol) in anhydrous ethanol (20 mL), which was subsequently heated to reflux and held for 5 hours. Upon completion of the reaction, the reaction mixture was concentrated under reduced pressure to remove the solvent and then diluted with ethyl acetate (100 mL). The diluted solution was washed sequentially with saturated sodium bicarbonate solution and saturated brine to remove acidic impurities and inorganic salts. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated again under reduced pressure to give the crude product. The crude product was purified by column chromatography (eluent: ethyl acetate/hexane, gradient elution, 0/100 to 20/80) to finally obtain ethyl 2-(4-(trifluoromethoxy)phenyl)acetate (2.06 g, 91% yield) as a yellow oil.

References[1] Patent: US2011/136833, 2011, A1. Location in patent: Page/Page column 36
4-(TrifluoroMethoxy)benzeneacetic acid ethyl ester Preparation Products And Raw materials
Raw materials4-(TRIFLUOROMETHOXY)PHENYLACETIC ACID-->4-Trifluoromethoxyphenylboronic acid-->Ethanol-->Ethyl bromoacetate
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