Sodium methoxide
Template:Short description Template:Chembox
Sodium methoxide is the simplest sodium alkoxide. With the formula Template:Chem2, it is a white solid, which is formed by the deprotonation of methanol. It is a widely used reagent in industry and the laboratory. It is also a dangerously caustic base.
Preparation and structure
Sodium methoxide is prepared by treating methanol with sodium:
The reaction is so exothermic that ignition is possible. The resulting solution, which is colorless, is often used as a source of sodium methoxide, but the pure material can be isolated by evaporation followed by heating to remove residual methanol.
As a solid, sodium methoxide is polymeric, with sheet-like arrays of Template:Chem2 centers, each bonded to four oxygen centers.[1]
The structure, and hence the basicity, of sodium methoxide in solution depends on the solvent. It is a significantly stronger base in DMSO where it is more fully ionized and free of hydrogen bonding.[2]
Applications
Organic synthesis
Sodium methoxide is a routinely used base in organic chemistry, applicable to the synthesis of numerous compounds ranging from pharmaceuticals to agrichemicals.[2] As a base, it is employed in dehydrohalogenations and various condensations.[3] It is also a nucleophile for the production of methyl ethers.[4]
Industrial applications
Sodium methoxide is used as an initiator of anionic addition polymerization with ethylene oxide, forming a polyether with high molecular weight.[5] Biodiesel is prepared from vegetable oils and animal fats (fatty acid triglycerides) by transesterification with methanol to give fatty acid methyl esters (FAMEs). Sodium methoxide acts as a catalyst for this reaction, but will combine with any free fatty acids present in the oil/fat feedstock to form soap byproducts.Script error: No such module "Unsubst".
Stability
The solid hydrolyzes in water to give methanol and sodium hydroxide. Indeed, samples of sodium methoxide are often contaminated with sodium hydroxide, which is difficult to detect. The compound absorbs carbon dioxide from the air to form methanol and sodium carbonate, thus diminishing the alkalinity of the base.Script error: No such module "Unsubst".
Commercial batches of sodium methoxide show variable levels of degradation, and were a major source of irreproducibility when used in Suzuki reactions.[6]
Safety
Sodium methoxide is highly caustic and reacts with water to give methanol, which is toxic and volatile.
NFPA 704
The ratings for this substance vary widely.
| Rating | Template:NFPA 704 diamond | Template:NFPA 704 diamond | Template:NFPA 704 diamond | Template:NFPA 704 diamond | Template:NFPA 704 diamond |
|---|---|---|---|---|---|
| Source | State of Connecticut[7] | DuPont[8] | Pharmco AAPR[9] | ScienceLab[10] (Both ratings on same sheet) | |
See also
References
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- ↑ Template:OrgSynth
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