Trimethylsilyl iodide

Trimethylsilyl iodide

Names
Preferred IUPAC name Iodotri(methyl)silane
Other names Iodotrimethylsilane; TMSI; TMS-I; Jung reagent
Identifiers
CAS Number	16029-98-4
3D model (JSmol)	Interactive image
ChemSpider	76879
ECHA InfoCard	100.036.503
PubChem CID	85247
UNII	7A65KRZ6NV^Y
CompTox Dashboard (EPA)	DTXSID4065997
InChI InChI=1S/C3H9ISi/c1-5(2,3)4/h1-3H3 Key: CSRZQMIRAZTJOY-UHFFFAOYSA-N InChI=1/C3H9ISi/c1-5(2,3)4/h1-3H3 Key: CSRZQMIRAZTJOY-UHFFFAOYAB
SMILES I[Si](C)(C)C
Properties
Chemical formula	C3H9ISi
Molar mass	200.094 g·mol^−1
Appearance	Clear colorless liquid[1]
Density	1.406 g/mL[1]
Boiling point	106–109 °C (223–228 °F; 379–382 K)[1]
Hazards
Flash point	−31 °C (−24 °F; 242 K)[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Trimethylsilyl iodide (iodotrimethylsilane or TMSI) is an organosilicon compound with the chemical formula (CH₃)₃SiI. It is a colorless, volatile liquid at room temperature.

Preparation

Trimethylsilyl iodide may be prepared by the oxidative cleavage of hexamethyldisilane by iodine[2] or by the cleavage of hexamethyldisiloxane with aluminium triiodide.[2][3]

TMS-TMS + I₂ → 2 TMSI (TMS = (CH₃)₃Si)

3 TMS-O-TMS + 2 AlI₃ → 6 TMSI + Al₂O₃

Applications

Trimethylsilyl iodide is used to introduce the trimethylsilyl group onto alcohols (ROH):

R-OH + TMSI → R-OTMS + HI

This type of reaction may be useful for gas chromatography analysis; the resultant silyl ether is more volatile than the underivatized original materials.[4] However, for the preparation of bulk trimethylsilylated material, trimethylsilyl chloride may be preferred due to its lower cost.

TMSI reacts with alkyl ethers (ROR′), forming silyl ethers (ROSiMe₃) and iodoalkanes (RI) that can be hydrolyzed to alcohols (ROH).[5]

Trimethylsilyl iodide is also used for the removing of the Boc protecting group,[2][6][7] especially where other deprotection methods are too harsh for the substrate.[8]

References

1. Michael E. Jung, Michael J. Martinelli, George A. Olah, G. K. Surya Prakash, Jinbo Hu (October 15, 2005). "Iodotrimethylsilane". Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.ri043.pub2. ISBN 978-0471936237. {{cite book}}: |journal= ignored (help)
2. Olah, G; Narang, S. C. (1982). "Iodotrimethylsilane—a versatile synthetic reagent". Tetrahedron. 38 (15): 2225. doi:10.1016/0040-4020(82)87002-6.
3. Michael E. Jung; Mark A. Lyster (1988). "Cleavage of Methyl Ethers with Iodotrimethylsilane: Cyclohexanol from Cyclohexyl Methyl Ether". Organic Syntheses; Collected Volumes, vol. 6, p. 353.
4. "GC/MS Analysis for Morphine and Other Opiates in Urine" (PDF).
5. Michael E. Jung; Mark A. Lyster (1977). "Quantitative dealkylation of alkyl ethers via treatment with trimethylsilyl iodide. A new method for ether hydrolysis". J. Org. Chem. 42 (23): 3761–3764. doi:10.1021/jo00443a033.
6. Michael E. Jung; Mark A. Lyster (1978). "Conversion of alkyl carbamates into amines via treatment with trimethylsilyl iodide". J. Chem. Soc., Chem. Commun. (7): 315–316. doi:10.1039/C39780000315.
7. Richard S. Lott; Virander S. Chauhan; Charles H. Stammer (1979). "Trimethylsilyl iodide as a peptide deblocking agent". J. Chem. Soc., Chem. Commun. (11): 495–496. doi:10.1039/C39790000495.
8. Zhijian Liu; Nobuyoshi Yasuda; Michael Simeone; Robert A. Reamer (2014). "N-Boc Deprotection and Isolation Method for Water-Soluble Zwitterionic Compounds". J. Org. Chem. 79 (23): 11792–11796. doi:10.1021/jo502319z. PMID 25376704.