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194673-12-6

194673-12-6 Structure

194673-12-6 Structure
IdentificationBack Directory
[Name]

ethyl 6-oxo-2-(trifluoromethyl)-1,4,5,6-tetrahydropyridine-3-carboxylate
[CAS]

194673-12-6
[Synonyms]

6-oxo-2-(trifL
Ethyl 6-oxo-2-(trifluoromethyl)
)-1,4,5,6-tetrahydro-3-pyridinecarboxyL
-1,4,5,6-tetrahydropyridine-3-carboxylate
3-Pyridinecarboxylicacid, 1,4,5,6-tetrahydro-6-oxo-2-(triflu...
Ethyl 2-oxo-6-(trifluoromethyl)-3,4-dihydro-1h-pyridine-5-carboxylate
ethyl 6-oxo-2-(trifluoromethyl)-1,4,5,6-tetrahydropyridine-3-carboxylate
6-Hydroxy-2-trifluoromethyl-4,5-dihydropyridine-3-carboxylic acid ethyl ester
2-oxo-6-(trifluoromethyl)-3,4-dihydro-1H-pyridine-5-carboxylic acid ethyl ester
1,4,5,6-Tetrahydro-6-oxo-2-(trifluoromethyl)-3-pyridinecarboxylic acid ethyl ester
3-Pyridinecarboxylicacid, 1,4,5,6-tetrahydro-6-oxo-2-(trifluoromethyl)-, ethyl ester
ethyl 6-oxo-2-(trifluoromethyl)-1,4,5,6-tetrahydropyridine-3-carboxylate ISO 9001:2015 REACH
[Molecular Formula]

C9H10F3NO3
[MDL Number]

MFCD00975005
[MOL File]

194673-12-6.mol
[Molecular Weight]

237.18
Chemical PropertiesBack Directory
[Melting point ]

128~130℃
[Boiling point ]

294℃
[density ]

1.351
[Fp ]

132℃
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

11.80±0.60(Predicted)
[Appearance]

Off-white to light yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

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

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

ethyl 6-oxo-2-(trifluoromethyl)-1,4,5,6-tetrahydropyridine-3-carboxylate(194673-12-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

Acrylamide

79-06-1

Ethyl 4,4,4-trifluoroacetoacetate

372-31-6

ethyl 6-oxo-2-(trifluoromethyl)-1,4,5,6-tetrahydropyridine-3-carboxylate

194673-12-6

GENERAL STEPS: A mixture of ethyl 4,4,4-trifluoroacetoacetate (14.7 mL, 0.1 mol, 1.6 eq.), acrylamide (4.5 g, 0.063 mol, 1.0 eq.), and p-toluene sulfonate (0.156 g, 0.82 mmol, 0.013 eq.) in toluene (60 mL) was refluxed in a Dean-Stark device for for 38 hours to azeotropically remove the resulting water. Upon completion of the reaction, most of the toluene was removed by slow distillation at atmospheric pressure and the reaction mixture was concentrated to a smaller volume. Toluene (60 mL) was added again to the concentrated mixture and the distillation and concentration process was repeated as described above. This operation was performed three times. Finally, the reaction mixture was further concentrated under vacuum and the resulting solid residue was purified by fast column chromatography (silica gel as stationary phase, eluent gradient: from hexane/ethyl acetate 9:1 to hexane/ethyl acetate 8:2). Purification afforded the target compound ethyl 6-oxo-2-(trifluoromethyl)-1,4,5,6-tetrahydro-3-pyridinecarboxylate as a brown solid (3.8 g, 25% yield). The product was analyzed by LC-MS (ESI+) and showed molecular ion peaks MH+: 238, 210, 190.

[References]

[1] Patent: WO2005/74939, 2005, A1. Location in patent: Page/Page column 40; 44
[2] Patent: WO2004/29026, 2004, A1. Location in patent: Page 33-34
[3] Patent: WO2004/29027, 2004, A1. Location in patent: Page 30
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