|Jmol-3D images||Image 1|
|Molar mass||108.64 g/mol|
|Appearance||Colorless liquid, fumes in moist air|
|Density||0.856 g/cm3, liquid|
|Melting point||−40 °C (233.2 K)|
|Boiling point||57 °C (330.2 K)|
|Solubility in water||reacts|
|Molecular shape||tetrahedral at Si|
|EU classification||Flammable (F)
|R-phrases||R11, R14, R20, R21, R35, R37|
|S-phrases||S16, S26, S36, S37, S39, S45|
|Flash point||−28 °C (−18 °F; 245 K)|
|Related halosilanes||Trimethylsilyl fluoride
|Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)|
|(what is: / ?)|
Trimethylsilyl chloride, also known as chlorotrimethylsilane is an organosilicon compound (silyl halide), with the formula (CH3)3SiCl, often abbreviated Me3SiCl or TMSCl. It is a colourless volatile liquid that is stable in the absence of water. It is widely used in organic chemistry.
TMSCl is prepared on a large scale by the Direct process, the reaction of methyl chloride with a silicon-copper alloy. The principal target of this process is dimethyldichlorosilane, but substantial amounts of the trimethyl and monomethyl products are also obtained. The relevant reactions are (Me = CH3):
- x MeCl + Si → Me3SiCl, Me2SiCl2, MeSiCl3, other products
Typically about 2-4% or the product stream is the monochloride, which forms an azeotrope with MeSiCl3.
Reactions and uses
TMSCl is reactive toward nucleophiles, resulting in the replacement of the chloride. In a characteristic reaction of TMSCl, the nucleophile is water, resulting in hydrolysis to give the hexamethyldisiloxane:
- 2 Me3SiCl + H2O → Me3Si-O-SiMe3 + 2 HCl
The related reaction of trimethylsilyl chloride with alcohols can be exploited to produce anhydrous solutions of hydrochloric acid in alcohols, which find use in the mild synthesis of esters from carboxylic acids and nitriles as well as, acetals from ketones. Similarly, trimethylsilyl chloride is also used to silanize laboratory glassware, making the surfaces more lipophilic.
Silylation in organic synthesis
By the process of silylation, polar functional groups such as alcohols and amines readily undergo reaction with trimethylsilyl chloride, giving trimethylsilyl ethers and trimethylsilyl amines. These new groups "protect"s the original functional group by removing the labile protons and decreasing the basicity of the heteroatom. The lability of the Me3Si-O and Me3Si-N groups can later be removed ("deprotected"). Trimethylsilylation can also be used to increase the volatility of a compound, enabling gas chromatography of normally nonvolatile substances such as glucose. Trimethylsilyl chloride also reacts with metal acetylides to give trimethylsilyl alkynes such as bis(trimethylsilyl)acetylene. Such derivatives are useful protected forms of alkynes.
In the presence of triethylamine and lithium diisopropylamide, enolisable aldehydes, ketones and esters are converted to trimethylsilyl enol ethers. Despite their hydrolytic instability, these compounds have found wide application in organic chemistry; oxidation of the double bond by epoxidation or dihydroxylation can be used to return the original carbonyl group with an alcohol group at the alpha carbon. The trimethylsilyl enol ethers can also be used as masked enolate equivalents in the Mukaiyama aldol addition.
Trimethylsilyl chloride is used to prepare other trimethylsilyl halides and pseudohalides, including trimethylsilyl fluoride, trimethylsilyl bromide, trimethylsilyl iodide, trimethylsilyl cyanide, trimethylsilyl azide, and trimethylsilyl trifluoromethanesulfonate (TMSOTf). These compounds are produced by an salt metathesis reaction between trimethylsilyl chloride and a salt of the (pseudo)halide (MX):
- MX + Me3Si-Cl → MCl + Me3Si-X
- 3 Me3SiCl + 3 Li + 1/2 N2 → (Me3Si)3N + 3 LiCl
Reduction of trimethylsilyl chloride give hexamethyldisilane:
- 2 Me3SiCl + 2 Na → 2 NaCl + Me3Si-SiMe3
- Röshe, L.; John, P.; Reitmeier, R. (2005), "Organic Silicon Compounds", Ullmann's Encyclopedia of Industrial Chemistry, Weinheim: Wiley-VCH, doi:10.1002/14356007.a24_021
- Such as in Norbert Zander and Ronald Frank (2005), The use of polystyrylsulfonyl chloride resin as a solid supported condensation reagent for the formation of esters: Synthesis of N-[(9-fluorenylmethoxy)carbonyl]-L-aspartic acid; α tert-butyl ester, β-(2-ethyl[(1E)-(4-nitrophenyl)azo]phenyl]amino]ethyl ester, Org. Synth. 81: 235
- Yoshihiko Ito, Shotaro Fujii, Masashi Nakatuska, Fumio Kawamoto, and Takeo Saegusa (1979), One-Carbon Ring Expansion of Cycloalkanones to Conjugated Cycloalkenone: 2-Cyclohepten-1-one, Org. Synth. 59: 113; Coll. Vol. 1: 327
- L. Birkofer and P. Wegner (1970), Trimethylsilyl azide, Org. Synth. 50: 107; Coll. Vol. 6: 1030
- Brook, Michael A. (2000). Silicon in Organic, Organometallic, and Polymer Chemistry. New York: John Wiley & Sons. pp. 193–194.