Trimethylsilyl cyanide

Trimethylsilyl cyanide is the chemical compound with the formula (CH3)3SiCN. This volatile liquid consists of a cyanide group, that is CN, attached to a trimethylsilyl group. The molecule is used in organic synthesis as the equivalent of hydrogen cyanide. It is prepared by the reaction of lithium cyanide and trimethylsilyl chloride:[1]

LiCN + (CH3)3SiCl → (CH3)3SiCN + LiCl
Trimethylsilyl cyanide
Names
IUPAC name
trimethylsilylformonitrile
Other names
Cyanotrimethylsilane; TMS cyanide; Trimethylsilylnitrile; Trimethylsilanecarbonitrile' Trimethylsilylcarbonitrile
Identifiers
3D model (JSmol)
Abbreviations TMSCN
ChemSpider
ECHA InfoCard 100.028.780
Properties
C4H9NSi
Molar mass 99.208 g·mol−1
Density 0.793 g/mL at 20 °C
Melting point 8 to 11 °C (46 to 52 °F; 281 to 284 K)
Boiling point 114 to 117 °C (237 to 243 °F; 387 to 390 K)
hydrolyzes
Solubility organic solvents
1.392
Hazards
R-phrases (outdated) R11 R26/27/28 R29
S-phrases (outdated) S16 S36/37/39 S45
Flash point 1 °C (34 °F; 274 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)
Infobox references

Structure

The molecule exhibits the expected structure of a nitrile-like compound. The compound exists in a facile equilibrium with a small amount of the isomeric isocyanide (CH3)3SiNC.[2] By contrast, the nearly isostructural tert-butyl nitrile does not readily isomerize to tert-butyl isocyanide.

Reactions

Trimethylsilyl cyanide hydrolyzes to give hydrogen cyanide and trimethylsilanol:

(CH3)3SiCN + H2O → (CH3)3SiOH + HCN

In its principal application, it adds across carbon-oxygen double bonds, for example in an aldehyde, to form a new carbon-carbon bond:

RCH=O + (CH3)3SiC≡N → N≡C–CHR–OSi(CH3)3

The product is an O-silylated cyanohydrin.

One use of this reagent is to convert pyridine-N-oxides into 2-cyanopyridine. This transformation is best done in dichloromethane solution using dimethylcarbamoyl chloride as the activating electrophile. It is possible to use benzoyl chloride but the yields and regioselectivity of the addition of the cyano group are lower.

Safety

This chemical is rated as "Fatal if swallowed, in contact with skin or if inhaled" as it hydrolyzes in the presence of moisture to give hydrogen cyanide gas.

Disposal by using dilute solution of alkali hydroxide is recommended.[3]

gollark: Why not an ewe bee stack?
gollark: Is it a ewe bee priority queue or just a regular ewe bee queue?
gollark: ubq = uniquely binomial qualifiers
gollark: Some languages don't have "characters" in the same way.
gollark: Unicode does not actually define "characters".

References
  1. Livinghouse, T. (1990). "Trimethylsilyl Cyanide: Cyanosilation of p-Benzoquinone". Organic Syntheses.; Collective Volume, 7, p. 517
  2. Booth, M. R.; Frankiss, S. G. (1968). "Trimethylsilyl isocyanide". Chem. Commun. (21): 1347–1348. doi:10.1039/C19680001347.
  3. MSDS of trimethylsilyl cyanide. (PDF). Gelest. [Jun 13, 2019]
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.