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Trimethylsilyl cyanide

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Trimethylsilyl cyanide Basic information

Product Name:
Trimethylsilyl cyanide
Synonyms:
  • TRIMETHYLSILYL CYANIDE FOR SYNTHESIS
  • trimethylsilylformonitrile
  • trimethylsilylmethanenitrile
  • trimethyl-silanecarbonitril
  • trimethylsilycyanide
  • TMSCN
  • TRIMETHYLSILANECARBONITRILE
  • TRIMETHYLSILYL CYANIDE
CAS:
7677-24-9
MF:
C4H9NSi
MW:
99.21
EINECS:
231-657-3
Product Categories:
  • Si (Classes of Silicon Compounds)
  • Si-(C)4 Compounds
  • Silicon Compounds (for Synthesis)
  • Synthetic Organic Chemistry
  • Small molecule
  • Building Blocks
  • C1 to C5
  • Chemical Synthesis
  • Cyanides/Nitriles
  • Nitrogen Compounds
  • Organic Building Blocks
Mol File:
7677-24-9.mol
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Trimethylsilyl cyanide Chemical Properties

Melting point:
8-11 °C(lit.)
Boiling point:
114-117 °C(lit.)
Density 
0.793 g/mL at 20 °C(lit.)
refractive index 
n20/D 1.392(lit.)
Flash point:
34 °F
storage temp. 
0-6°C
solubility 
Miscible with organic solvents.
form 
liquid
color 
Yellow
Specific Gravity
0.744
Water Solubility 
reacts
Sensitive 
Moisture Sensitive
Hydrolytic Sensitivity
8: reacts rapidly with moisture, water, protic solvents
BRN 
1737612
InChIKey
LEIMLDGFXIOXMT-UHFFFAOYSA-N
CAS DataBase Reference
7677-24-9(CAS DataBase Reference)
EPA Substance Registry System
Silanecarbonitrile, trimethyl- (7677-24-9)
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Safety Information

Hazard Codes 
F,T+,T,N
Risk Statements 
11-26/27/28-29-50/53
Safety Statements 
16-36/37/39-45-61-28A-26
RIDADR 
UN 3384 6.1/PG 1
WGK Germany 
3
10-21
Hazard Note 
Highly Flammable/Toxic
TSCA 
Yes
HazardClass 
6.1
PackingGroup 
II
HS Code 
29310095

MSDS

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Trimethylsilyl cyanide Usage And Synthesis

Chemical Properties

Trimethylsilyl cyanide (TMSCN) is a commercial reagent used as cyanide source for nucleophilic reactions. It is a clear colorless to yellow liquid, moisture sensitive, with a boiling point of 114–117 °C, which was first synthetized by the reaction of trimethylsilicon halides TMSX and AgCN in 1952.

TMSCN is a versatile reagent that can be used in several different reactions, but it is generally used in nucleophilic additions to aldehydes, ketones and imines to form cyanohydrin silyl ethers (Scheme 1a) and α-aminonitriles in Strecker-type reactions (Scheme 1b).

Uses

Reacts with aldehydes and ketones to give cyanohydrin-TMS ethers which can be reduced to β-aminoethyl alcohols.
Trimethylsilyl cyanide (TMSCN)  participates in carbonyl aminomethylation via α-silyloxy nitriles.
TMSCN can be used as a reagent in the:
Trimethylsilyl cyanide was used in the second step of an oxidative Michael addition of cyanide anion to Baylis–Hillman adducts. The importance of the addition of cyanide to α,β-unsaturated carbonyl derivatives is that the products can be converted into a variety of compounds including γ-aminobutyric acids. The reaction took place in a liquid ionic medium ([bmim]Br), which was reused several times without losing its activity. The β-cyano carbonyl compounds were obtained with high regioselectivity and yields (>79%).

Cyanosilylation of carbonyl compounds using various catalysts.
Synthesis of α-aminonitriles by one-pot, three-component Strecker reaction of ketones with various amines using Brønsted acid catalyst.
Cyanation of aryl halides using palladium-complex as a catalyst.

Uses

Trimethylsilyl Cyanide is used as a reagent in the synthesis of optically active cyanohydrins. Used in the preparation of Reissert compounds, which represent reactive polyamides. Toxic to humans.

Preparation

Trimethylsilyl cyanide, (CH3)3 Si-CN, is obtained by reacting trimethylsilyl chloride with an approximately equimolar amount of an alkali metal cyanide in the absence of water and in the presence of catalytic, sub-stoichiometric amounts of both an alkali metal iodide and N-methylpyrrolidone, at a temperature of from 15°-25° C.
Trimethylsilyl cyanide is very toxic. All reactions in this sequence should be carried out in a hood.
Preparation of trimethylsilyl cyanide
TRIMETHYLSILYL CYANIDE: CYANOSILATION OF p-BENZOQUINONE

Reactions

Trimethylsilyl cyanide is a useful silicon reagent which reacts readily with aldehydes and ketones in the presence of catalytic amounts of Lewis acids or of cyanide ion, to give the trimethylsilyl ethers of the corresponding cyanohydrins (Evans,Carroll and Truesdale,1974).Even normally unreactive ketones react readily with trimethylsilyl cyanide due to the formation of the strong Si-O bond which displaces the equilibrium in favour of the derivative.The reaction provides a valuable alternative to the base-catalysed addition of hydrogen cyanide to carbonyl compounds which often gives only poor yields.Tetralone,for example,is reported not to form a cyanohydrin, but it gives a trimethylsilyl derivative in excellent yield.The silylated cyanohydrins can be hydrolysed to a-hydroxy acids(Corey, Crouse and Anderson,1975) and on reduction with lithium aluminium hydride they afford the corresponding 3-amino alcohols in excellent yield.This sequence provides a better route to these valuable intermediates (they are used in the ring expansion of cyclo- alkanones)than the classical methods through reaction of hydrogen cyanide or nitromethane with the carbonyl compound.The derivatives from aromatic aldehydes are excellent acyl anion equivalents and have been used in 'umpolung' conversion of aldehydes into ketones and acyloins by reaction of the derived anions with alkyl halides and aldehydes or ketones (Deuchert et al,1979;Hnig and Wehner,1979).

Purification Methods

The material should have only one sharp signal in the 1H NMR (in CCl4 with CHCl3 as internal standard) : 0.4ppm and IR with max at 2210cm1 [McBride & Beachall J Am Chem Soc 74 5247 1952, Prober J Am Chem Soc 77 3224 1955]; otherwise purify it by fractionating through an 18 x 1/4inch column. [Evers et al. J Am Chem Soc 81 4493 1959.] It has also been carefully distilled using a 60cm vacuum jacketed column. If the volume of sample is small, the cyanide can be chased (in the distillation) with xylene that had been previously distilled over P2O5. It is HIGHLY TOXIC and FLAMMABLE. [Evans et al. J Org Chem 39 914 1974, Beilstein 4 IV 3893.]

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