Identification | Back Directory | [Name]
ETHYL 4-(TRIFLUOROMETHYL)PHENYL ACETATE | [CAS]
721-63-1 | [Synonyms]
2-[4-(trifluoroMethyl)phenyl]butanoate Ethyl 4-(trifluoromethyl)benzeneacetate ETHYL 4-(TRIFLUOROMETHYL)PHENYL ACETATE ethyl 2-(4-(trifluoromethyl)phenyl)acetate REF DUPL: Ethyl 4-(trifluoromethyl)phenylacetate 4-(Trifluoromethyl)benzeneacetic acid ethyl ester (4-TRIFLUOROMETHYL-PHENYL)-ACETIC ACID ETHYL ESTER Benzeneacetic acid, 4-(trifluoroMethyl)-, ethyl ester | [Molecular Formula]
C11H11F3O2 | [MDL Number]
MFCD07779351 | [MOL File]
721-63-1.mol | [Molecular Weight]
232.2 |
Chemical Properties | Back Directory | [Melting point ]
34-35 °C | [Boiling point ]
104-105 °C(Press: 7 Torr) | [density ]
1.207 | [storage temp. ]
Sealed in dry,Room Temperature | [solubility ]
soluble in Methanol | [form ]
Solid | [color ]
Colorless |
Hazard Information | Back Directory | [Synthesis]
General procedure: Under standard Schlenk operating conditions, the reaction system is first evacuated and backfilled three times with dry pure nitrogen. To a pre-dried Schlenk tube fitted with a magnetic stirring bar, palladium catalyst (see Tables 1 to 4 for specific types and amounts), ligand (see Tables 1 to 4), N,N-dimethylpyridin-4-amine (DMAP, see Tables 1 to 4), and monoethyl malonate potassium salt (see Tables 1 to 4) are added sequentially. Subsequently, the reaction tube was evacuated and backfilled with argon, and this process was repeated three times. Under argon protection, p-bromobenzotrifluoride (see Tables 1 through 4) and an appropriate amount of solvent (see Tables 1 through 4) were added via syringe. The reaction tube was sealed and stirred for 10 minutes at room temperature. Afterwards, the reaction tube is connected to a Schlenk line pre-filled with argon and placed in an oil bath preheated to 140-150°C and the reaction is stirred for 20-25 hours. After completion of the reaction, the reaction was cooled to room temperature, the reaction mixture was diluted with ether and the yield of ethyl 4-(trifluoromethyl)phenylacetate was determined by gas chromatography using 1,3-dimethoxybenzene as an internal standard. | [References]
[1] Tetrahedron, 2012, vol. 68, # 9, p. 2113 - 2120 |
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