Ethyl (trimethylsilyl)acetate Chemical Properties

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)

Safety Information

Risk Statements 

10

Safety Statements 

16-24/25

RIDADR 

UN 3272 3/PG 3

WGK Germany 

3

F 

10-21

TSCA 

Yes

HazardClass 

3

PackingGroup 

III

HS Code 

29319090

MSDS

• Language:English Provider:SigmaAldrich
• Language:English Provider:ALFA

Ethyl (trimethylsilyl)acetate Usage And Synthesis

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(4071-88-9)Related Product Information

• Azidotrimethylsilane
• POLY(VINYL ACETATE)
• ETHYL (METHYLTHIO)ACETATE
• Hexamethyldisilazane
• N-(Trimethylsilyl)acetamide
• Ethyl nitroacetate
• Methyl acetate
• Trimethylsilylacetylene
• Sodium acetate
• Lithium bis(trimethylsilyl)amide
• Ethyl trifluoroacetate
• Tocopheryl acetate
• Ethyl phenylacetate
• Glatiramer acetate
• Ethyl acetate
• Vinyl acetate
• N-(Trimethylsilyl)imidazole
• Ethyl chloroacetate