|  | |  |  | Phenyl trifluoromethanesulfonate Basic information | 
 | Product Name: | Phenyl trifluoromethanesulfonate |  | Synonyms: | PHENYL TRIFLUOROMETHANESULFONATE;PHENYL TRIFLATE;Phenol triflate;Phenol trifluoromethanesulfonate;Trifluoromethanesulfonic acid phenyl ester;Trifluoromethylsulfonyloxybenzene;Trifluoromethanesulfonic Acid Phenyl Ester
Phenyl Triflate;Phenyl trifluoromethanesulfonate 98% |  | CAS: | 17763-67-6 |  | MF: | C7H5F3O3S |  | MW: | 226.17 |  | EINECS: |  |  | Product Categories: |  |  | Mol File: | 17763-67-6.mol |  |  | 
|  |  | Phenyl trifluoromethanesulfonate Chemical Properties | 
 | Boiling point | 99-100 °C/60 mmHg (lit.) |  | density | 1.396 g/mL at 25 °C (lit.) |  | refractive index | n20/D 1.435(lit.) |  | Fp | 160 °F |  | storage temp. | Inert atmosphere,Room Temperature |  | form | clear liquid |  | color | Colorless to Almost colorless | 
|  |  | Phenyl trifluoromethanesulfonate Usage And Synthesis | 
 | Chemical Properties | Colorless Liquid. 
 |  | Uses | Phenyl trifluoromethanesulfonate (phenyl triflate) may be used in the following studies: As an arylating agent for the asymmetric α-arylation of ketones catalyzed by Pd(dba)2 and difluorphos.
 As a reactant in the one pot synthesis of carbazoles by palladium-catalyzed N-arylation of anilines with phenyl triflate followed by oxidative coupling.
 Synthesis of N-(2,6-diarylbenzoyl)anilines by diarylation of benzanilides with phenyl triflate in the presence of palladium-based catalyst.
 As an arylating agent in the synthesis of (R)-2-phenyl-2,3-dihydrofuran by the arylation of 2,3-dihydrofuran.
 |  | Preparation | Synthesis of Phenyl trifluoromethanesulfonate: The reaction of phenol (1.00 g, 10.6 mmol) with triflic anhydride as outlined in the general procedure provided phenyl trifluoromethanesulfonate as colorless oil (0.73 g, 30%). 1H NMR (400 MHz, CDCl3) δ 7.50 – 7.42 (m, 2H), 7.41 – 7.36 (m, 1H), 7.32 – 7.24 (m, 2H).
 |  | General Description | Phenyl trifluoromethanesulfonate (phenyl triflate) is an aryl fluorosulphonate. It has been synthesized by the reaction of phenol with fluorosulphonic anhydride. | 
|  |  | Phenyl trifluoromethanesulfonate Preparation Products And Raw materials | 
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