Trimethylsilyl group

Short description: Functional group

A trimethylsilyl group (abbreviated TMS) is a functional group in organic chemistry. This group consists of three methyl groups bonded to a silicon atom [−Si(CH3)3], which is in turn bonded to the rest of a molecule. This structural group is characterized by chemical inertness and a large molecular volume, which makes it useful in a number of applications.

A trimethylsilyl group bonded to a methyl group forms tetramethylsilane, which is abbreviated as TMS as well.

Compounds with trimethylsilyl groups are not normally found in nature. Chemists sometimes use a trimethylsilylating reagent to derivatize rather non-volatile compounds such as certain alcohols, phenols, or carboxylic acids by substituting a trimethylsilyl group for a hydrogen in the hydroxyl groups on the compounds. This way trimethylsiloxy groups [−O-Si(CH3)3] are formed on the molecule. A couple of examples of trimethylsilylating agents include trimethylsilyl chloride and bis(trimethylsilyl)acetamide. Trimethylsilyl groups on a molecule have a tendency to make it more volatile, often making the compounds more amenable to analysis by gas chromatography or mass spectrometry. An example of such trimethylsilylation is mentioned in the Brassicasterol article. Such derivatizations are often done on a small scale in special vials.

When attached to certain functional groups in a reactant molecule, trimethylsilyl groups may also be used as temporary protecting groups during chemical synthesis or some other chemical reactions.

In chromatography, derivitization of accessible silanol groups in a bonded stationary phase with trimethylsilyl groups is referred to as endcapping.

In an NMR spectrum, signals from atoms in trimethylsilyl groups in compounds will commonly have chemical shifts close to the tetramethylsilane reference peak at 0 ppm. Also compounds, such as high temperature silicone "stopcock" grease, which have polysiloxanes (often called silicones) in them will commonly show peaks from their methyl groups (attached to the silicon atoms) having NMR chemical shifts close to the tetramethylsilane standard peak, such as at 0.07 ppm in CDCl3.[1]

Otherwise very reactive molecules can be isolated when enveloped by bulky trimethylsilyl groups. This effect can be observed in tetrahedranes.

## Contents

* 1 Super silyl groups
* 2 Alcohol protection
* 2.1 Most common protection methods
* 2.2 Most common deprotection methods
* 3 See also
* 4 References
* 5 External links

## Super silyl groups

the tri(trimethylsilyl)silyl group Tris(trimethylsilyl)silane: R=H

Related to trimethylsilyl groups are "super" silyl groups of which there exist two varieties: A silicon group connected to three trimethylsilyl groups makes a tri(trimethylsilyl)silyl group (TTMSS or TMS3Si) and a silicon group connected to three tert-butyl groups. The TTMSS group was proposed in 1993 by Hans Bock. With a van der Waals volume of up to 7 cubic angstrom it surpasses the related TIPS group (around 2)[2][3] and one potential application is its use as a temporary substituent promoting asymmetric induction for example in this diastereoselective one-pot reaction involving two sequential Mukaiyama aldol reactions:[4]

TTMSS can also stand for tris(trimethylsilyl)silane,[5][6] which is comparable as a chemical reagent to tributyltin hydride without the associated toxicity concern of organotin and tributyltin compounds.[7][8] The reagent is employed in radical reductions, hydrosilylation and consecutive radical reactions.[9]

## Alcohol protection

In organic synthesis, TMS group is used as a protecting group for alcohols.

### Most common protection methods

* Trimethylsilyl chloride (TMSCl) or trimethylsilyl trifluoromethanesulfonate (TMSOTf) and base (i.e. pyridine, triethylamine, or 2,6-lutidine) in dichloromethane[10][11][12][13][14]
* TMSCl and lithium sulfide (Li2S) in acetonitrile

### Most common deprotection methods

* TMS groups are susceptible to cleavage upon treatment with HF-based reagents
* Tetrabutylammonium fluoride (Bu4NF) in THF
* Fluorosilicic acid (H2SiF6)
* Treatment with HCl in THF/water solution

## See also

* Trimethylsilanol
* Trimethylsilylacetylene
* Trimethylsilyl chloride
* Tetramethylsilane
* Trimethylsilyl fluoride is a byproduct in preparing diethylaminosulfur trifluoride (DAST) from sulfur tetrafluoride:[15]

Et2NSiMe3 \+ SF4 → Et2NSF3 \+ Me3SiF

## References

1. ↑ Gottlieb, H. E.; Kotlyar, V.; Nudelman, A. NMR Chemical Shifts of Common Laboratory Solvents as Trace Impurities. J. Org. Chem. 1997, 62(21), pp 7512-7515. doi:10.1021/jo971176v
2. ↑ "Super Silyl" Group for Diastereoselective Sequential Reactions: Access to Complex Chiral Architecture in One Pot Matthew B. Boxer and Hisashi Yamamoto J. Am. Chem. Soc.; 2007; 129(10) pp 2762 - 2763; (Communication) doi:10.1021/ja0693542
3. ↑ Tris(trimethylsilyl)silyl-Governed Aldehyde Cross-Aldol Cascade Reaction Boxer, M. B.; Yamamoto, H. J. Am. Chem. Soc.; (Communication); 2006; 128(1); 48-49. doi:10.1021/ja054725k
4. ↑ The starting materials are acetaldehyde and benzophenone which are both converted to silyl enol ether by reaction with tris(trimethylsilyl)silane and triflic acid with evolution of hydrogen. The aldol reaction is catalyzed by bis(trifluoromethane)sulfonimide
5. ↑ "Tris(trimethylsilyl)silane 97%". Sigma-Aldrich Co. LLC.. http://www.sigmaaldrich.com/catalog/product/aldrich/360716. Retrieved 2014-05-05.
6. ↑ Chatgilialoglu, Chryssostomos; Ferreri, Carla; Landais, Yannick; Timokhin, Vitaliy I. (25 June 2018). "Thirty Years of (TMS)3SiH: A Milestone in Radical-Based Synthetic Chemistry". Chemical Reviews 118 (14): 6516–6572. doi:10.1021/acs.chemrev.8b00109. PMID 29938502.
7. ↑ Brook, Michael A. (2000). Silicon in Organic, Organometallic, and Polymer Chemistry. New York: John Wiley & Sons, Inc.. pp. 172–173.
8. ↑ "Tris(trimethylsilyl)silane, TTMSS". https://www.organic-chemistry.org/chemicals/reductions/tris(trimethylsilyl)silane-ttmss.shtm.
9. ↑ Recent Applications of the (TMS)3SiH Radical-Based Reagent, Chryssostomos Chatgilialoglu, Jacques Lalevée Molecules 2012, 17, 527-555; doi:10.3390/molecules17010527
10. ↑ Nicolaou, K. C.; Liu, J. J.; Hwang, C.-K.; Dai, W.-M.; Guy, R. K. (1992-01-01). "Synthesis of a fully functionalized CD ring system of taxol" (in en). Journal of the Chemical Society, Chemical Communications (16): 1118. doi:10.1039/c39920001118. ISSN 0022-4936. http://xlink.rsc.org/?DOI=c39920001118.
11. ↑ Nicolaou, K. C.; Yang, Zhen; Sorensen, Erik J.; Nakada, Masahisa (1993-01-01). "Synthesis of ABCtaxoid ring systems via a convergent strategy" (in en). Journal of the Chemical Society, Chemical Communications (12): 1024. doi:10.1039/c39930001024. ISSN 0022-4936. http://xlink.rsc.org/?DOI=c39930001024.
12. ↑ Nicolaou, K. C.; Hwang, C.-K.; Soresen, E. J.; Clairborne, C. F. (1992-01-01). "A convergent strategy towards taxol. A facile enantioselective entry into a fully functionalized ring A system" (in en). Journal of the Chemical Society, Chemical Communications (16): 1117. doi:10.1039/c39920001117. ISSN 0022-4936. http://xlink.rsc.org/?DOI=c39920001117.
13. ↑ Nicolaou, K. C.; Yang, Z.; Liu, J. J.; Ueno, H.; Nantermet, P. G.; Guy, R. K.; Claiborne, C. F.; Renaud, J. et al. (1994-02-17). "Total synthesis of taxol" (in en). Nature 367 (6464): 630–634. doi:10.1038/367630a0. PMID 7906395. Bibcode: 1994Natur.367..630N.
14. ↑ Nicolaou, K. C.; Claiborne, Christopher F.; Nantermet, Philippe G.; Couladouros, Elias A.; Sorensen, Erik J. (1994-02-01). "Synthesis of Novel Taxoids". Journal of the American Chemical Society 116 (4): 1591–1592. doi:10.1021/ja00083a063. ISSN 0002-7863.
15. ↑ W. J. Middleton, E. M. Bingham "Diethylaminosulfur Trifluoride" Organic Syntheses, Coll. Vol. 6, p.440; Vol. 57, p.50. Online version

## External links

* Identification of Silylation Artifacts in Derivatization Reactions for Gas Chromatography

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