Trimethylsilylacetylene

Trimethylsilylacetylene

Names
IUPAC name ethynyltrimethylsilane
Identifiers
CAS Number	1066-54-2 Y
3D model (Jmol)	Interactive image
ChemSpider	59499 Y
ECHA InfoCard	100.012.655
PubChem	66111
InChI InChI=1S/C5H10Si/c1-5-6(2,3)4/h1H,2-4H3 Y Key: CWMFRHBXRUITQE-UHFFFAOYSA-N Y InChI=1S/C5H10Si/c1-5-6(2,3)4/h1H,2-4H3 InChI=1S/C5H10Si/c1-5-6(2,3)4/h1H,2-4H3 Key: CWMFRHBXRUITQE-UHFFFAOYSA-N
SMILES C#C[Si](C)(C)C
Properties
Chemical formula	C5H10Si
Molar mass	98.22 g·mol−1
Appearance	colorless liquid
Density	0.69 g/mL
Boiling point	53 °C (127 °F; 326 K)
Hazards
Safety data sheet	External MSDS
EU classification (DSD)	F
R-phrases	R11
S-phrases	S16 S24/25 S29 S33 S9
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)
Infobox references

Trimethylsilylacetylene is an acetylene molecule protected on one end by the trimethylsilyl group. It is popularly used in alkynylations, e.g. the Sonogashira reaction. After desilylation (e.g. with TBAF), the ethynyl group is introduced. Using a protected alkyne, as opposed to acetylene gas, prevents further (undesired) coupling reactions and also has the benefit of being a liquid.

This compound 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.^[1]

References

1. ↑ Andrew B. Holmes and Chris N. Sporikou (1993). "Trimethylsilylacetylene". Org. Synth. ; Coll. Vol., 8, p. 606