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Trimethylsilylacetylene

Trimethylsilylacetylene is the acetylene HC2Si(CH3)3. It is a colorless liquid. Called 'tms acetylene', it is used as a source of 'HC2−'. The trimethylsilyl group protected can be desilyated with TBAF. Using this protected alkyne, as opposed to acetylene itself, prevents further coupling reactions and also has the benefit of being a liquid. A less expensive alternative reagent is 2-methylbut-3-yn-2-ol, which after alkynylation is deprotected with base. Trimethylsilylacetylene is the acetylene HC2Si(CH3)3. It is a colorless liquid. Called 'tms acetylene', it is used as a source of 'HC2−'. The trimethylsilyl group protected can be desilyated with TBAF. Using this protected alkyne, as opposed to acetylene itself, prevents further coupling reactions and also has the benefit of being a liquid. A less expensive alternative reagent is 2-methylbut-3-yn-2-ol, which after alkynylation is deprotected with base. Trimethylsilylacetylene is commercially available. It may also be prepared in a manner similar to other silyl compounds: deprotonation of acetylene with a Grignard reagent, followed by reaction with trimethylsilyl chloride.

[ "Catalysis" ]
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