ChemicalBook--->CAS DataBase List--->262608-88-8

262608-88-8

262608-88-8 Structure

262608-88-8 Structure
IdentificationBack Directory
[Name]

2-FLUORO-4-(TRIFLUOROMETHYL)CINNAMIC ACID
[CAS]

262608-88-8
[Synonyms]

RARECHEM AL BK 0319
2-FLUORO-4-(TRIFLUOROMETHYL)CINNAMIC ACID
3-(2-Fluoro-4-(trifluoromethyl)phenyl)acrylic acid
2-Propenoic acid, 3-[2-fluoro-4-(trifluoromethyl)phenyl]-
(E)-3-2-Fluoro-4-(trifluoromethyl)phenylprop-2-enoic acid
(E)-3-[2-fluoro-4-(trifluoromethyl)phenyl]-2-propenoic acid
[Molecular Formula]

C10H6F4O2
[MDL Number]

MFCD00236292
[MOL File]

262608-88-8.mol
[Molecular Weight]

234.15
Chemical PropertiesBack Directory
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

Flame Over Circle (GHS03)
GHS03
[Signal word ]

Warning
[Hazard statements ]

H272-H303
[Precautionary statements ]

P221-P270-P280-P301+P312-P370+P378r-P403-P501c
[Hazard Codes ]

Xi
[HazardClass ]

IRRITANT
[HS Code ]

2916399090
Spectrum DetailBack Directory
[Spectrum Detail]

2-FLUORO-4-(TRIFLUOROMETHYL)CINNAMIC ACID(262608-88-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

Malonic acid

141-82-2

2-FLUORO-4-(TRIFLUOROMETHYL)BENZALDEHYDE

89763-93-9

2-FLUORO-4-(TRIFLUOROMETHYL)CINNAMIC ACID

262608-88-8

Example 3: General procedure for the synthesis of 3-(2-fluoro-4-(trifluoromethyl)phenyl)acrylic acid from malonic acid and 2-fluoro-4-(trifluoromethyl)benzaldehyde. A mixture of 5.0 g (26.0 mmol) of 2-fluoro-4-(trifluoromethyl)benzaldehyde, 3.10 g (29.8 mmol) of malonic acid, 0.26 g (3.0 mmol) of piperidine, and 15 ml of pyridine was heated to reflux temperature until the release of carbon dioxide ceased (about 3 hours). After completion of the reaction, it was cooled to room temperature and the reaction mixture was poured into a mixture of 300 g of ice and 100 ml of 6N HCl. The precipitate was separated, washed twice sequentially with water and n-heptane and dried. 5.2 g (85% yield) of 3-(2-fluoro-4-(trifluoromethyl)phenyl)acrylic acid was obtained.1H-NMR (400MHz, D6-DMSO): δ= 6.73 (d, J = 16.1Hz, 1H, 2-H), 7.63 (d, 1H, 5'-H), 7.65 (d, J = 16.1Hz, 1H, 3-H), 7.76 (d , 1H, 3'-H), 8.07 (dd, 1H, 6'-H), 12.8 (br, 1H, COOH).

[References]

[1] Patent: US2005/38091, 2005, A1. Location in patent: Page column 6
[2] Patent: US2005/267179, 2005, A1. Location in patent: Page/Page column 15; 16
[3] Patent: WO2008/26149, 2008, A1. Location in patent: Page/Page column 22-23
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