ChemicalBook--->CAS DataBase List--->4270-70-6

4270-70-6

4270-70-6 Structure

4270-70-6 Structure
IdentificationMore
[Name]

Triphenylsulfonium chloride
[CAS]

4270-70-6
[Synonyms]

TRIPHENYLSULFONIUM CHLORIDE
’triphenylsulfoniumchloride’solution
Sulfonium,triphenyl-,chloride
triphenyl-sulfoniuchloride
triphenylsulfurchloride
triphenylsulphonium chloride
triphenylsulfonium ion
Triphenylsulfoniumchlorid
[EINECS(EC#)]

224-259-6
[Molecular Formula]

C18H15ClS
[MDL Number]

MFCD00031716
[Molecular Weight]

298.83
[MOL File]

4270-70-6.mol
Chemical PropertiesBack Directory
[Melting point ]

277 °C
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[Water Solubility ]

Soluble in water.
[CAS DataBase Reference]

4270-70-6(CAS DataBase Reference)
[EPA Substance Registry System]

4270-70-6(EPA Substance)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
[WGK Germany ]

3
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Chlorotrimethylsilane-->Phenyl sulfoxide-->Chlorobenzene-->Tetrahydrofuran
Hazard InformationBack Directory
[Uses]

Triphenylsulfonium chloride is used as a key intermediate that is widely used in the new electronic chemicals such as semiconductor, LCD and TFT.
[Preparation]

Triphenylsulfonium Chloride Synthesis: Diphenyl sulfoxide, 40 g (0.2 mole), was dissolved in 400 g of dichloroethane, which was stirred under ice cooling. At a temperature below 20° C., 65 g (0.6 mole) of trimethylsilyl chloride was added dropwise to the solution, which was aged for 30 minutes at the temperature. Then, a Grignard reagent which had been prepared from 14.6 g (0.6 mole) of metallic magnesium, 67.5 g (0.6 mole) of chlorobenzene and 168 g of tetrahydrofuran (THF) was added dropwise at a temperature below 20° C. The reaction solution was aged for one hour, after which 50 g of water at a temperature below 20° C. was added to quench the reaction. To this solution, 150 g of water, 10 g of 12N hydrochloric acid, and 200 g of diethyl ether were further added.
The water layer was separated and washed with 100 g of diethyl ether, yielding an aqueous solution of triphenylsulfonium chloride. The compound in aqueous solution form was used in the subsequent reaction without further isolation.
Spectrum DetailBack Directory
[Spectrum Detail]

Triphenylsulfonium chloride(4270-70-6)1HNMR
Triphenylsulfonium chloride(4270-70-6)FT-IR
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

Triphenylsulfonium chloride, 94%(4270-70-6)
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