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208517-35-5

208517-35-5 Structure

208517-35-5 Structure
IdentificationBack Directory
[Name]

2-(TRIFLUOROMETHYL)-3-PYRIDINECARBOXYLIC ACID ETHYL ESTER
[CAS]

208517-35-5
[Synonyms]

Ethyl 2-(trifluoromethyl)nicotinate
2-Trifluoromethyl-nicotinic acid ethyl ester
ethyl 2-(trifluoroMethyl)pyridine-3-carboxylate
2-(TRIFLUOROMETHYL)-3-PYRIDINECARBOXYLIC ACID ETHYL ESTER
2-(TRIFLUOROMETHYL)-3-PYRIDINECARBOXYLIC ACID ETHYL ESTER ISO 9001:2015 REACH
[EINECS(EC#)]

1312995-182-4
[Molecular Formula]

C9H8F3NO2
[MDL Number]

MFCD08741365
[MOL File]

208517-35-5.mol
[Molecular Weight]

219.16
Chemical PropertiesBack Directory
[Boiling point ]

235.8±40.0 °C(Predicted)
[density ]

1.284±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[pka]

-1.38±0.22(Predicted)
[Appearance]

Colorless to light yellow Liquid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2933399990
Hazard InformationBack Directory
[Chemical Properties]

Yellow liquid
[Synthesis]

2,4-Pentadienoic acid, 5-(diMethylaMino)-2-(2,2,2-trifluoroacetyl)-, ethyl ester

1146961-22-9

2-(TRIFLUOROMETHYL)-3-PYRIDINECARBOXYLIC ACID ETHYL ESTER

208517-35-5

In a 1 L single neck round bottom flask equipped with a magnetic stirrer and a reflux condenser, ethyl (2E,4E)-5-(dimethylamino)-2-(2,2,2-trifluoroacetyl)penta-2,4-dienoate (80.50 g, 303.8 mmol) was dissolved in a solvent mixture of methanol (700 mL) and 25% aqueous ammonia solution (240 mL). The reaction mixture was heated to 70 °C and maintained for 20 minutes. It was then cooled to room temperature and the methanol was removed by distillation under reduced pressure. The residue was diluted with water (200 mL) and extracted with ether (2 x 300 mL). The organic phases were combined, washed with saturated brine (200 mL), dried over anhydrous magnesium sulfate and filtered. The solvent was evaporated under reduced pressure to give 65.0 g of red oily crude product. The crude product was pure enough for subsequent reactions. For further purification, the crude product was filtered through a short silica gel column, followed by evaporation of the filtrate to give 59.9 g of light yellow flowing oil in 90% yield.

[References]

[1] Patent: WO2009/54742, 2009, A2. Location in patent: Page/Page column 13-14
Spectrum DetailBack Directory
[Spectrum Detail]

2-(TRIFLUOROMETHYL)-3-PYRIDINECARBOXYLIC ACID ETHYL ESTER(208517-35-5)1HNMR
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