PHENYL 2-(TRIMETHYLSILYL)ETHYL SULFONE
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
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
Safety Information
- Safety Statements
- 22-24/25
- WGK Germany
- 3
- HS Code
- 29310099
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
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.]