Basic information Safety Supplier Related

PHENYL 2-(TRIMETHYLSILYL)ETHYL SULFONE

Basic information Safety Supplier Related

PHENYL 2-(TRIMETHYLSILYL)ETHYL SULFONE Basic information

Product Name:
PHENYL 2-(TRIMETHYLSILYL)ETHYL SULFONE
Synonyms:
  • PHENYL 2-(TRIMETHYLSILYL)ETHYL SULFONE
  • (2-Phenylsulfonylethyl)trimethylsilane
  • PHENYL 2-(TRIMETHYLSILYL)ETHYL SULFONE, 99+%
  • 1-(phenylsulfonyl)-2-(trimethylsilyl)ethane
  • 1-(Phenylsulfonyl)-2-(trimethylsilyl)ethane, 2-(Phenylsulfonyl)ethyltrimethylsilane, 2-(Trimethylsilyl)ethyl phenyl sulfone
  • Benzene, [[2-(trimethylsilyl)ethyl]sulfonyl]-
  • Trimethyl(2-(Phenylsulfonyl)Ethyl)Silane
CAS:
73476-18-3
MF:
C11H18O2SSi
MW:
242.41
Mol File:
73476-18-3.mol
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PHENYL 2-(TRIMETHYLSILYL)ETHYL SULFONE Chemical Properties

Melting point:
51-52 °C(lit.)
Boiling point:
347.4±34.0 °C(Predicted)
Density 
1.040±0.06 g/cm3(Predicted)
Flash point:
>230 °F
solubility 
sol all common ethereal, halocarbon, and hydrocarbon solvents.
form 
solid
CAS DataBase Reference
73476-18-3
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Safety Information

Safety Statements 
22-24/25
WGK Germany 
3
HS Code 
29310099

MSDS

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PHENYL 2-(TRIMETHYLSILYL)ETHYL SULFONE Usage And Synthesis

Chemical Properties

white fine crystalline powder

Physical properties

mp 52 °C.

Uses

(2-Phenylsulfonylethyl)trimethylsilane is widely used as reagent for the synthesis of mono- and 1,1-disubstituted alkenes via sulfone metalation, alkylation, and fluoride-induced elimination.
A sequence involving metalation, alkylation, and fluoride-induced elimination of benzenesulfinate allows the conversion of (2) to a terminal alkene. An analogous sequence involving a double alkylation of (2) provides a 1,1-disubstituted alkene (eq 2). The lithio derivative of (2) has also been used to prepare cyclopropylidene derivatives, homoallylic alcohols, and allyl silanes via the Julia alkenation.

Preparation

(2-phenylsulfonylethyl)trimethylsilane (2) is prepared by radical addition of thiophenol to vinyltrimethylsilane to give (2-phenylthioethyl)trimethylsilane (1), which is then oxidized with hydrogen peroxide).

Purification Methods

Dissolve it in Et2O, wash it with saturated HCO 3 followed by saturated NaCl, H2O and dried (MgSO4). Evaporation leaves residual crystals with m 52o. [Hsiao & Shechter Tetrahedron Lett 23 1963 1982, Bortolini et al. J Org Chem 53 2688 1985.]

PHENYL 2-(TRIMETHYLSILYL)ETHYL SULFONESupplier

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