ETHYL 4-(TRIFLUOROMETHYL)PHENYL ACETATE
ETHYL 4-(TRIFLUOROMETHYL)PHENYL ACETATE Basic information
- Product Name:
- ETHYL 4-(TRIFLUOROMETHYL)PHENYL ACETATE
- Synonyms:
-
- ETHYL 4-(TRIFLUOROMETHYL)PHENYL ACETATE
- ethyl 2-(4-(trifluoromethyl)phenyl)acetate
- REF DUPL: Ethyl 4-(trifluoromethyl)phenylacetate
- 4-(Trifluoromethyl)benzeneacetic acid ethyl ester
- 2-[4-(trifluoroMethyl)phenyl]butanoate
- Benzeneacetic acid, 4-(trifluoroMethyl)-, ethyl ester
- (4-TRIFLUOROMETHYL-PHENYL)-ACETIC ACID ETHYL ESTER
- Ethyl 4-(trifluoromethyl)benzeneacetate
- CAS:
- 721-63-1
- MF:
- C11H11F3O2
- MW:
- 232.2
- Mol File:
- 721-63-1.mol
ETHYL 4-(TRIFLUOROMETHYL)PHENYL ACETATE Chemical Properties
- 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
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38
- Safety Statements
- 26-36/37/39
- HS Code
- 2916340000
ETHYL 4-(TRIFLUOROMETHYL)PHENYL ACETATE Usage And Synthesis
Synthesis
402-43-7
6148-64-7
721-63-1
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
ETHYL 4-(TRIFLUOROMETHYL)PHENYL ACETATESupplier
- Tel
- 18210857532; 18210857532
- jkinfo@jkchemical.com
- Tel
- 400-6106006
- saleschina@alfa-asia.com
- Tel
- 021-67121386
- Sales-CN@TCIchemicals.com
- Tel
- 847-367-3680
- sales@arkpharminc.com
- Tel
- 001-857-928-2050 or 1-888-588-9418
- sales@chemreagents.com
ETHYL 4-(TRIFLUOROMETHYL)PHENYL ACETATE(721-63-1)Related Product Information
- 4-(Trifluoromethyl)phenyl acetate
- 4-(Trifluoromethyl)phenylacetic acid
- Ethyl phenylacetate
- RARECHEM AL BI 1336
- ETHYL 4-(TRIFLUOROMETHYL)PHENYL ACETATE
- 6-CHLORO-2,3-DIFLUORO-4-(TRIFLUOROMETHYL)PHENYLACETIC ACID ETHYL ESTER
- ETHYL 2-FLUORO-4-(TRIFLUOROMETHYL)PHENYLACETATE
- ETHYL 2-[2,4-BIS(TRIFLUOROMETHYL)PHENYL]-2-OXOACETATE
- (S)-2-(2'-OXOCYCLOHEXYL)-2-(4''-TRIFLUOROMETHYLPHENYL)GLYCOLIC ACID ETHYL ESTER
- 3,3,4,4,4-PENTAFLUORO-2-HYDROXY-2-[4-(TRIFLUOROMETHYL)PHENYL]BUTYRIC ACID ETHYL ESTER
- RARECHEM AL BW 0991
- 2,3,6-TRIFLUORO-4-(TRIFLUOROMETHYL)PHENYLACETIC ACID ETHYL ESTER
- ETHYL OXO-(4-TRIFLUOROMETHYLPHENYL)ACETATE
- ETHYL ALPHA-CYANO-2-NITRO-4-(TRIFLUOROMETHYL)PHENYLACETATE
- 3,3,3-TRIFLUORO-2-HYDROXY-2-(4-TRIFLUOROMETHYLPHENYL)PROPIONIC ACID ETHYL ESTER
- ETHYL 3,5-BIS(TRIFLUOROMETHYL)PHENYL ACETATE