Ethidene was introduced at the position of C17 of DHEA by Wittig reaction to getsteroid D. When potassium tert-butoxide was used as alkali, the reaction reached theyield of 95.0%; sodium hydride being as alkali and the yield 66.0%.
In the experiment,sodium amide, sodium triphenyl methane, and sodium tert-butoxide are selected as catalyst for synthesis of instead 2-cyano-2-(p-nitro phenyl)ethyl acetate to displace the high dangerous catalyst sodium hydride.
Three compounds of 2-fluoro-4-(trans-4-alkylcyclohexyl)phenylboronic acid were synthesized using 1-(trans-4-alkylcyclohexyl)-3-fluorobenzene,n-butyllithium,tributyl borate,and potassium tert-butoxide as reactants,their yields were 52%~56%,and their structures were confirmed by IR and ~1HNMR.
4,12-dibromo[2,2]paracyclophane is allowed to react with benzophenone imine in sodium tert-butoxide base and Pd-DPPFcatalyst to produce 4-benzophnoni mine- 12-bromo[2,2]paracyclophane
The key intermediate for the synthesis was 2-O acetyl-3, 4-di-O-benzyl 6-deoxy-a-L-talopyra nosyl chloride, which was converted into the target compound by ring closure with potassium tert-butoxide.
The condensation reactions of α,α-diacetyl ketene dithioacetals with arylaldehydes catalyzed by sodium tert-butoxide were performed. These reactions were affected by the alkylthio groups.
A system aluminum (and titanium) tert-butoxide-tert-butyl hydroperoxide (1 : 2) under mild conditions (20 °C, 1 h) oxidizes aliphatic and alkylaromatic sulfides and diphenyl sulfide to the corresponding sulfones in yields close to ~100%.
The title compound was synthesized from L-rhamnose by a series of steps. The key intermediate for the synthesis was 2-O acetyl-3, 4-di-O-benzyl 6-deoxy-a-L-talopyra nosyl chloride, which was converted into the target compound by ring closure with potassium tert-butoxide. The 1H NMR spectrum of the anhydro sugar was determined by the use of single frequency decoupling. The new compounds obtained in the synthesis were identified by their 1H NMR spectra,elemental analysis,mass spectra and optical r...
Methyl (3,5 di tert butyl 4 hydroxyphenyl) propionate,an intermediate for the preparation of tetrakis [3 (3,5 di t butyl 4 hydroxyphenyl) propionyloxymethyl] methane by one step method,was synthesized with 2,6 di tert buty phenol and methyl acrylate in the presence of potassium tert butoxide in a 15 liter stainless batch tank reactor.The optimum technological conditions were determined and excellent yield and selectivity w...
The reaction of producing potassium tert butoxide from potash and tert butyl alcohol is an intensive reversible reaction.Because the reaction equilibrium favors the formation of alcohol,potassium tert butoxide can not be obtained without removing the water formed during the reaction.So a technology integrating azeotropic reaction distillation in boundary film and a packed column having large surface area is applied.The ...