ChemicalBook > CAS DataBase List > Ethyl (trimethylsilyl)acetate
Ethyl (trimethylsilyl)acetate
- Product Name
- Ethyl (trimethylsilyl)acetate
- CAS No.
- 4071-88-9
- Chemical Name
- Ethyl (trimethylsilyl)acetate
- Synonyms
- ETSA;2-trimethylsilylbutanoate;Ethyl(Trimethylsily)Acetate;ETHYL (TRIMETHYLSILYL)ACETATE;ETHYL(2-TRIMETHYLSILYL)ACETATE;ETHYL TRI METHYLSILYLACETATE 99%;Ethyl (trimethylsilyl)acetate,97%;Ethyl acetatethree Methylsilicone;Ethyl (trimethylsilyl)acetate, 98+%;(TRIMETHYLSILYL)ACETIC ACID ETHYL ESTER
- CBNumber
- CB7271085
- Molecular Formula
- C7H16O2Si
- Formula Weight
- 160.29
- MOL File
- 4071-88-9.mol
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Ethyl (trimethylsilyl)acetate Property
- Boiling point:
- 156-159 °C (lit.)
- Density
- 0.876 g/mL at 25 °C (lit.)
- refractive index
- n20/D 1.415(lit.)
- Flash point:
- 95 °F
- storage temp.
- Inert atmosphere,Room Temperature
- solubility
- sol ethereal and chlorinated solvents; reacts with protic solvents.
- form
- clear liquid
- color
- Colorless to Almost colorless
- Specific Gravity
- 0.876
- Water Solubility
- Decomposition
- Hydrolytic Sensitivity
- 2: reacts with aqueous acid
- Sensitive
- Moisture Sensitive
- BRN
- 1755902
- CAS DataBase Reference
- 4071-88-9(CAS DataBase Reference)
- NIST Chemistry Reference
- Ethyl (trimethylsilyl)acetate(4071-88-9)
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Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H226Flammable liquid and vapour
- Precautionary statements
-
P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.
P240Ground/bond container and receiving equipment.
P241Use explosion-proof electrical/ventilating/lighting/…/equipment.
P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.
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N-Bromosuccinimide Price
Sigma-Aldrich
- Product number
- 209120
- Product name
- Ethyl trimethylsilylacetate
- Purity
- ≥98%
- Packaging
- 25g
- Price
- $244
- Updated
- 2022/05/15
TCI Chemical
- Product number
- T1584
- Product name
- Ethyl (Trimethylsilyl)acetate
- Purity
- >93.0%(GC)
- Packaging
- 5g
- Price
- $54
- Updated
- 2024/03/01
TCI Chemical
- Product number
- T1584
- Product name
- Ethyl (Trimethylsilyl)acetate
- Purity
- >93.0%(GC)
- Packaging
- 25g
- Price
- $162
- Updated
- 2024/03/01
Alfa Aesar
- Product number
- A17707
- Product name
- Ethyl (trimethylsilyl)acetate, 98+%
- Packaging
- 10g
- Price
- $59.65
- Updated
- 2024/03/01
Alfa Aesar
- Product number
- A17707
- Product name
- Ethyl (trimethylsilyl)acetate, 98+%
- Packaging
- 50g
- Price
- $257
- Updated
- 2024/03/01
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Ethyl (trimethylsilyl)acetate Chemical Properties,Usage,Production
Chemical Properties
Ethyl trimethylsilylacetate is a clear colorless liquid. It is stable to the usual manipulations, and can be stored in glass containers for years without change of physical and spectral properties.
Uses
(silylating agent; source of an ethyl acetate anion equivalent.Ethyl trimethylsilylacetate is reactive to nucleophiles and readily undergoes desilylation reactions with acid or alkali,ethanol, and bromine.
Uses
Ethyl trimethylsilylacetate is used in the synthesis of ethyl-2,2-dibromo-2-(trimethylsilyl)acetate and α,β-unsaturated esters. It was also used to silylate the enolizable aldehydes and ketones.
Preparation
ethyl trimethylsilylacetate synthesis: Available by a Reformatsky reaction from ethyl bromoacetate, and by reaction of trimethylsilylmethylmagnesium chloride with ethyl chloroformate. An alternative approach requires the treatment of ethyl acetate with triphenylmethylsodium followed by chlorotrimethylsilane The use of a nitrogen base with ethyl acetate in THF followed by reaction with chlorotrimethylsilane results in a mixture of C- and O-silylation. The use of HMPA as additive in the reaction medium increases the amount of O-silylation to 90%. Similar methods can be used to prepare analogs.
General Description
Reaction of ethyl trimethylsilylacetate (ETSA) with dilute hydrochloric acid, dilute alkali, anhydrous HCl, anhydrous bromine and absolute ethanol has been reported. ETSA undergoes condensation with aromatic aldehydes in the presence of base catalyst to yield β-trimethylsiloxycarboxylates. Lithium ETSA reacts with ketones to yield α,β-unsaturated esters.
Purification Methods
Purify it by distilling ca 10g of reagent through a 15cm, Vigreux column (p 11) and then redistilling it through a 21cm glass helices-packed column [Hauze & Hauser J Am Chem Soc 75 994 1953]. Alternatively, dissolve it in Et2O, wash with H2O, dilute Na2CO3, dry over Na2CO3, evaporate Et2O, and distil it through a column of 15 theoretical plates. [Gold et al. J Am Chem Soc 70 2874 1948, Beilstein 4 IV 3974.]
Ethyl (trimethylsilyl)acetate Preparation Products And Raw materials
Raw materials
Preparation Products
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View Lastest Price from Ethyl (trimethylsilyl)acetate manufacturers
Career Henan Chemical Co
- Product
- Ethyl (trimethylsilyl)acetate 4071-88-9
- Price
- US $1.00/g
- Min. Order
- 1g
- Purity
- 99%
- Supply Ability
- 1000KGS
- Release date
- 2019-12-20
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