4071-85-6 Usage
Description
Trimethylsilylketene is a versatile and reactive chemical compound known for its various applications in organic synthesis. It is characterized by its boiling point of 81-82 °C and a density of 0.80 g/cm3.
Uses
1. Used in Organic Synthesis:
Trimethylsilylketene is used as a reactive acylating agent for amines and alcohols, facilitating the formation of various organic compounds.
2. Used in Pharmaceutical Industry:
Trimethylsilylketene is used as a building block for the synthesis of coumarins, which are important in the development of pharmaceutical compounds.
3. Used in Chemical Research:
Trimethylsilylketene is used in the synthesis of α-silyl ketones via the addition of organocerium reagents, contributing to the advancement of chemical research.
4. Used in Material Science:
Trimethylsilylketene is used in the treatment with stabilized ylides to form trimethylsilyl-substituted allenes, which are valuable in the development of new materials.
5. Used in Synthesis of β-Lactones:
Trimethylsilylketene is used in a cycloaddition with aldehydes to afford β-lactones, which are important intermediates in the synthesis of various organic compounds.
6. Used in Synthesis of Small Rings:
Trimethylsilylketene is used to form small rings with diazomethane, which are useful in the development of complex organic molecules.
7. Used in Synthesis of Heterocycles:
Trimethylsilylketene is used in the treatment with n-BuLi to form a ketene enolate, which is a key step in the synthesis of heterocycles.
8. Used in Trimethylsilylacetylation of Alcohols and Amines:
Trimethylsilylketene is used in the acetylation of alcohols and amines, providing a method for the protection of these functional groups in organic synthesis.
9. Used in Synthesis of Coumarins via Cyclization-Elimination:
Trimethylsilylketene is used in the cyclization-elimination process to synthesize coumarins, which are important in the pharmaceutical and chemical industries.
10. Used in One-pot Formation of α-Silyl Ketones:
Trimethylsilylketene is used in a one-pot reaction to form α-silyl ketones, simplifying the synthesis process and increasing efficiency.
11. Used in Reaction with Diazomethane to Form Silylated Cyclopropanes and Cyclobutanones:
Trimethylsilylketene is used in reactions with diazomethane to form silylated cyclopropanes and cyclobutanones, which are valuable in the synthesis of complex organic molecules.
12. Used in Formation of the Ketene Enolate:
Trimethylsilylketene is used in the formation of the ketene enolate, which is an important intermediate in various organic reactions.
Preparation
Most often prepared (eq 1) by pyrolysis
of ethoxy(trimethylsilyl)acetylene at 120°C (100 mmol scale,
65% yield).Recently, pyrolysis of t-butoxy(trimethylsilyl)
acetylene has been shown to be a convenient alternative for
the preparation of trimethylsilylketene (1). Thermal decomposition
of t-butoxy(trimethylsilyl)acetylene causes elimination
of 2-methylpropene slowly at temperatures as low as 50°C and
instantaneously at 100–110°C (30 mmol scale, 63% yield).
The main advantage of this method is that it is possible to generate
trimethylsilylketene in the presence of nucleophiles, leading
to in situ trimethylsilylacetylation (eq 2). Increased shielding
of the triple bond prevents problems such as polymerization
and nucleophilic attack that occur when the ketene is generated
in situ from (trimethylsilyl)ethoxyacetylene. Trimethylsilylketene
can also be prepared (eq 3) via the dehydration
of commercially available trimethylsilylacetic acid with 1,3-
dicyclohexylcarbodiimide (DCC) in the presence of a catalytic
amount of triethylamine (100 mmol scale, 63%). Other
typical methods used for ketene generation such as dehydrohalogenation
of the acyl chloride and pyrolysis of the
anhydride have been applied to the preparation of (1);
however, both methods afford low yields.There have been no significant developments in the methods
used to prepare trimethylsilylketene (TMSK). However,
Black et al. have published slight modifications. to the original
preparation by Ruden, which primarily deals with accessing
ethoxyacetylene.
Check Digit Verification of cas no
The CAS Registry Mumber 4071-85-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,7 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4071-85:
(6*4)+(5*0)+(4*7)+(3*1)+(2*8)+(1*5)=76
76 % 10 = 6
So 4071-85-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H10OSi/c1-7(2,3)5-4-6/h5H,1-3H3
4071-85-6Relevant articles and documents
Intramolecular Dehydration of Dialkylacetic Acids and Trimethylsilylacetic Acid with Dicyclohexylcarbodiimide to the Corresponding Stable Ketenes
Olah, George A.,Wu, An-hsiang,Farooq, Omar
, p. 568 (1989)
A new, simple preparation for stable dialkyl ketenes involving intramolecular dehydration of appropriately substituted acetic acids with dicyclohexylcarbodiimide (DCC) in the presence of catalytic amounts of triethylamine gives 60-70percent yield of the corresponding ketenes.Trimethylsilylacetic acid also gives trimethylsilylketene in good yield.
The formation of silylated β-lactams from silylketenes through Lewis acid promoted [2+2] cycloaddition: A combined theoretical and experimental study
Pelotier, Beatrice,Rajzmann, Michel,Pons, Jean-Marc,Campomanes, Pablo,Lopez, Ramon,Sordo, Tomas L.
, p. 2599 - 2606 (2007/10/03)
The stereoselective formation of silylated cis-β-lactams from (trimethylsilyl)ketene and an α-imino ester by Lewis acid catalysis is described. Theoretical results suggest that the reaction between (trimethylsilyl)ketene and trans- (methoxycarbonyl)-N-methylformaldimine would proceed most favourably with the BF3 catalyst coordinated to the ketene. Moreover, the calculated energy barriers account for the cis:trans ratio found experimentally. ( Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005).
C2-Symmetric Cu(II) Complexes as Chiral Lewis Acids. Catalytic, Enantioselective Cycloadditions of Silyl Ketenes
Evans, David A.,Janey, Jacob M.
, p. 2125 - 2128 (2007/10/03)
(matrix presented) C2-Symmetric bis(oxazoline)-Cu(II) complexes (4a-g) catalyze the enantioselective [2 + 2] cycloaddition between (silyl)ketenes and chelating carbonyl substrates. A range of substituted β-lactones can be produced in excellent yields and selectivities. It was also found that (trimethylsilyl)-ketene (1) may also undergo a highly selective hetero Diels-Alder reaction with β,γ-unsaturated α-keto esters.
