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Sodium ethoxide is commonly used as a base in the Claisen condensation [7] and malonic ester synthesis. [8] Sodium ethoxide may either deprotonate the α-position of an ester molecule, forming an enolate, or the ester molecule may undergo a nucleophilic substitution called transesterification. If the starting material is an ethyl ester, trans ...
Barbital, then called "Veronal", was first synthesized in 1902 by German chemists Emil Fischer and Joseph von Mering, who published their discovery in 1903. [2] Barbital was prepared by condensing diethylmalonic ester with urea in the presence of sodium ethoxide, or by adding at least two molar equivalents of ethyl iodide to the silver salt of malonylurea (barbituric acid) or possibly to a ...
For example, treating 2-Bromo-2-methyl butane with sodium ethoxide in ethanol produces the Zaytsev product with moderate selectivity. [9] Due to steric interactions, a bulky base – such as potassium tert-butoxide, triethylamine, or 2,6-lutidine – cannot readily abstract the proton that would lead to the Zaytsev product. In these situations ...
Sodium ethoxide; T. Tantalum(V) ethoxide; Titanium ethoxide; V. Vinyltriethoxysilane This page was last edited on 4 July 2018, at 11:07 (UTC). ...
A classic case is sodium methoxide produced by the addition of sodium metal to methanol: [citation needed] 2 CH 3 OH + 2 Na → 2 CH 3 ONa + H 2. Other alkali metals can be used in place of sodium, and most alcohols can be used in place of methanol. Generally, the alcohol is used in excess and left to be used as a solvent in the reaction.
If an alkoxide such as sodium ethoxide is used as base, deprotonation takes place only to the extent of about 0.1% because acetone is a weaker acid than ethanol (pK a = 16). If, however, a more powerful base such as sodium hydride (NaH) or lithium diisopropylamide ( LDA ) is used, a carbonyl compound can be completely converted into its enolate ...
Amobarbital (formerly known as amylobarbitone or sodium amytal as the soluble sodium salt) is a drug that is a barbiturate derivative. It has sedative-hypnotic properties. It is a white crystalline powder with no odor and a slightly bitter taste. It was first synthesized in Germany in 1923. It is considered a short to intermediate acting ...
In practice, considerable sodium is consumed by the formation of hydrogen. [citation needed] For this reason, an excess of sodium is often required. Because the hydrolysis of sodium is rapid, not to mention dangerous, the Bouveault-Blanc reaction requires anhydrous ethanol and can give low yields with insufficiently dry ethanol.