Ethyl (trimethylsilyl)acetate

Ethyl (trimethylsilyl)acetate Structure
Ethyl (trimethylsilyl)acetate structure
Common Name Ethyl (trimethylsilyl)acetate
CAS Number 4071-88-9 Molecular Weight 160.286
Density 0.9±0.1 g/cm3 Boiling Point 157.5±0.0 °C at 760 mmHg
Molecular Formula C7H16O2Si Melting Point N/A
MSDS Chinese USA Flash Point 35.0±0.0 °C
Symbol GHS02
GHS02
Signal Word Warning

Synthesis of alpha,alpha-dibromo esters as precursors of ynolates.

Chem. Pharm. Bull. 51(4) , 477-78, (2003)

Aliphatic alpha,alpha-dibromo esters, precursors of ynolates, were synthesized via bromination of lithium alpha-bromo ester enolates with 1,2-dibromotetrafluoroethane in good yields. alpha-Trimethylsilyl-alpha,alpha-dibromo esters were synthesized via radical...

External chiral ligand-mediated enantioselective Peterson reaction of alpha-trimethylsilanylacetate with substituted cyclohexanones.

Org. Lett. 4 , 4329, (2002)

[reaction: see text] The asymmetric Peterson reaction of an alpha-trimethylsilanylacetate with 4-substituted and 3,5-disubstituted cyclohexanones was mediated by an external chiral tridentate ligand to give the corresponding olefins with an axial chirality in...

Synth. Commun. 19 , 2441, (1989)

J. Chem. Soc. Perkin Trans. I , 3217, (1988)

Synthesis and Cleavage of Ethyl Trimethylsilylacetate1, 2. Gold JR, et al.

J. Am. Chem. Soc. 70(9) , 2874-76, (1948)

New synthesis of. alpha.,. beta.-unsaturated carboxylic esters. Shimoji K, et al.

J. Am. Chem. Soc. 96(5) , 1620-21, (1974)

P. Albaugh-Robertson, J.A.Katzenellenbogen

J. Org. Chem. 48 , 5288, (1983)

T.V. RajanBabu

J. Org. Chem. 49 , 2083, (1984)

I. Kuwajima et al.

Organic Synth. 61 , 122, (1983)