Phenyl trifluoromethanesulfonate

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 Structure
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
Safety Information
Hazard Codes T
Risk Statements 36/37/38-34-24/25
Safety Statements 26-36-45-36/37/39
RIDADR UN 2927 6.1/PG 2
WGK Germany 3
HS Code 29049090
MSDS Information
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SigmaAldrich English
Phenyl trifluoromethanesulfonate Usage And Synthesis
Chemical PropertiesColorless Liquid.
UsesPhenyl 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.
PreparationSynthesis 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 DescriptionPhenyl 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
Preparation Products4-Nitrophenylboronic acid pinacol ester-->N-PHENYL-3-BIPHENYLAMINE-->R-3,3'-Bis(phenyl)-1,1'-bi-2-naphthol-->4-PHENYL-3-BUTYN-1-OL-->1-PHENYLCYCLOPENTENE-->3-HYDROXYBENZOPHENONE-->Methyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate-->Phenylpentane
P-TOLYL TRIFLATE 4-ACETYLPHENYL TRIFLATE CATECHOL BIS(TRIFLUOROMETHANESULFONATE) 3,5-DIMETHOXYPHENOL TRIFLUOROMETHANESULFONATE (R)-(-)-1,1'-Binaphthol-2,2'-bis(trifluoromethanesulfonate) 8-QUINOLINYL TRIFLATE METHYL 2-TRIFLUOROMETHANESULFONYLOXY-1-NAPHTHOATE ETHYL 2-(TRIFLUOROMETHYL SULFONYLOXY) BENZOATE 2-FLUORO-4-[2-(4-PROPYLCYCLOHEXYL)ETHYL]PHENYL TRIFLUOROMETHANESULFONATE GMC 1-169 Phenyl trifluoromethanesulfonate 2-(TRIMETHYLSILYL)PHENYL TRIFLUOROMETHANESULFONATE 4,4-BIPHENOL BIS(TRIFLUOROMETHANESULFONATE) 4-NITROPHENYL TRIFLUOROMETHANESULFONATE 4-METHOXYPHENYL TRIFLUOROMETHANESULFONATE GMC 2-83 TRIFLUOROMETHANESULFONIC ACID 6-BROMO-2-NAPHTHYL ESTER 1-NAPHTHYL TRIFLATE

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