Trimethylsilyl iodide
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| Names | |||
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IUPAC name
Iodo(trimethyl)silane
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| Other names
Iodotrimethylsilane; TMSI; TMS-I; Jung reagent
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| Identifiers | |||
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3D model (JSmol)
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| ChemSpider | |||
| ECHA InfoCard | 100.036.503 | ||
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PubChem CID
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| Properties | |||
| C3H9ISi | |||
| Molar mass | 200.09 g·mol−1 | ||
| Appearance | Clear colorless liquid | ||
| Density | 1.406 g/mL | ||
| Boiling point | 106–109 °C (223–228 °F; 379–382 K) | ||
| Hazards | |||
| Flash point | −31 °C (−24 °F; 242 K) | ||
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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| 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.
Trimethylsilyl iodide may be prepared by the oxidative cleavage of hexamethyldisilane by iodine, or by the cleavage of hexamethyldisiloxane with aluminium triiodide.
Trimethylsilyl iodide is used to introduce the trimethylsilyl group onto alcohols (ROH):
This type of reaction may be useful for gas chromatography analysis; the resultant silyl ether is more volatile than the underivatized original materials. 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).
Trimethylsilyl iodide is also used for the removal of the Boc protecting group, especially where other deprotection methods are too harsh for the substrate.
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