Bis(trimethylsilyl)acetylene

From Wikipedia, the free encyclopedia
Bis(trimethylsilyl)acetylene
Skeletal formula of bis(trimethylsilyl)acetylene
Ball-and-stick model of the bis(trimethylsilyl)acetylene molecule
Names
Preferred IUPAC name
Ethynediylbis(trimethylsilane)
Other names
BTMSA
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.035.141 Edit this at Wikidata
  • InChI=1S/C8H18Si2/c1-9(2,3)7-8-10(4,5)6/h1-6H3 ☒N
    Key: ZDWYFWIBTZJGOR-UHFFFAOYSA-N ☒N
  • InChI=1/C8H18Si2/c1-9(2,3)7-8-10(4,5)6/h1-6H3
    Key: ZDWYFWIBTZJGOR-UHFFFAOYAF
  • C(#C[Si](C)(C)C)[Si](C)(C)C
Properties
C8H18Si2
Molar mass 170.402 g·mol−1
Appearance Colorless to white Liquid
Density 0.791 g/cm3
Melting point 26 °C (79 °F; 299 K)
Boiling point 134.6 ± 8.0 °C
0.031 g/L
Hazards
Main hazards Flammable, Irritant
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N  (what is checkY☒N ?)
Infobox references

Bis(trimethylsilyl)acetylene (BTMSA) is an organosilicon compound with the formula Me3SiC≡CSiMe3 (Me = methyl). It is a colorless liquid that is soluble in organic solvents. This compound is used as a surrogate for acetylene.

BTMSA is prepared by treating acetylene with butyl lithium followed by addition of chlorotrimethylsilane:[1][2]

Li2C2 + 2 Me3SiCl → Me3SiC≡CSiMe3 + 2 LiCl

Applications[]

BTMSA is used as a nucleophile in Friedel-Crafts type acylations and alkylations and a precursor to lithium trimethylsilylacetylide. The TMS groups can be removed with tetra-n-butylammonium fluoride (TBAF) and replaced with protons. BTMSA is also a useful reagent in cycloaddition reactions. Illustrating its versatility, BTMSA was used in a concise total synthesis of (±)-estrone.[3] A key step in this synthesis was the formation of the steroidal skeleton, catalyzed by CpCo(CO)2.

BTMSA also serves as a ligand in organometallic chemistry. For example, it forms stable adducts with metallocenes.[4]

Cp2TiCl2 + Mg + Me3SiC≡CSiMe3 → Cp2Ti[(CSiMe3)2] + MgCl2

BTMSA is also used in the total synthesis of epibatidine (and analogs), and also in the synthesis of iclaprim.

References[]

  1. ^ Holmes, A.; Sporikou, C.; Org. Synth. 1993, Coll. Vol. 8, 606.
  2. ^ Walton, D.R.M.; Waugh, F. (1972). "Friedel-crafts reactions of bis(trimethylsilyl)polyynes with acyl chlorides; a useful route to terminal-alkynyl ketones". Journal of Organometallic Chemistry. 37: 45–56. doi:10.1016/S0022-328X(00)89260-8.
  3. ^ Curtain, M. L.; Wang, C. Bis(trimethylsilyl) acetylene. e-EROS.
  4. ^ Rosenthal, Uwe; Burlakov, Vladimir V.; Arndt, Perdita; Baumann, Wolfgang; Spannenberg, Anke (2003). "The Titanocene Complex of Bis(trimethylsilyl)acetylene: Synthesis, Structure, and Chemistry†". Organometallics. 22 (5): 884–900. doi:10.1021/om0208570.
Retrieved from ""