Sodium methylsulfinylmethylide
 |
|
| Names | |
|---|---|
|
IUPAC name
Sodium methylsulfinylmethylide
|
|
| Other names
sodium dimsylate, dimsylsodium, NaDMSYL
|
|
| Identifiers | |
|
3D model (JSmol)
|
|
| Abbreviations | NaDMSO |
| ChemSpider | |
|
|
|
|
| Properties | |
| C2H5NaOS | |
| Molar mass | 100.13 |
| Appearance | White solid, may be apple-green or purple in solution |
| Reacts forming DMSO | |
| Solubility | Very soluble in DMSO and many polar organic solvents |
| Hazards | |
| Main hazards | decomposes to corrosive NaOH |
| Related compounds | |
|
Related compounds
|
Dimethyloxosulfonium methylide, dimethyl sulfoxide |
|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
|
 (what is   ?) |
|
| Infobox references | |
Sodium methylsulfinylmethylide (also called NaDMSO or dimsyl sodium) is the sodium salt of the conjugate base of dimethyl sulfoxide. This unusual salt has some uses in organic chemistry as a base and nucleophile.
Since the first publication in 1965 by Corey et al., a number of additional uses for this reagent have been identified.
Sodium methylsulfinylmethylide is prepared by heating sodium hydride or sodium amide in DMSO.
The pKa of DMSO is 35, which leads NaDMSO to be a powerful Brønsted base. NaDMSO is used in the generation of phosphorus and sulfur ylides. NaDMSO in DMSO is especially convenient in the generation of dimethyloxosulfonium methylide and dimethylsulfonium methylide.
NaDMSO condenses with esters (1) to form β-ketosulfoxides (2), which can be useful intermediates. Reduction of β-ketosulfoxides with aluminium amalgam gives methyl ketones (3). Reaction with alkyl halides followed by elimination gives α,β-unsaturated ketones (4). Interestingly, β-ketosulfoxides can also be used in the Pummerer rearrangement to introduce nucleophiles alpha to a carbonyl (5).
...
Wikipedia