The reaction conditions were optimized:n[1-(trans-4-alkylcyclohexyl)-3-fluorobenzene]∶n(potassium tert-butoxide)∶n(n-butyllithium)∶n(tributyl borate)=1∶2∶1.2∶1.5,reaction temperature-85~-90 ℃ and reaction time 2.5 h.
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.
Novel hole transporting material APB were synthesized with 9-bromoanthracene and arkylamine DPB as raw materials in the mixture catalyst of sodium tert-butoxide,Pd(OAc)_2/P(t-Bu) system.
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.
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%.
Fluoroalkyl iodide R_fI(1) [a R_f=CF_3(CF_2)_5; b R_f=(CF_2)_6Cl; c R_f=(CF_2)_4Cl; d R_f (CF_2)_2Cl; e R_f=CF_3(CF_2)_2; f R_f=H(CF_2)_4; g R_f=(CF_2)_4O(CF_2)_2SO_2F]reacted with trimethylsilylacetylene (2) in the presence of catalytic amounts of copper in acetonitril to give a mixture of E and Z-fluoroalkylated adducts, R_fCH=CISiMe_3 (3) in good yield. Reaction of a, ω-fluoroalkylene diiodide e.g. I(CF_2)_6I (4) with 2 under the similar conditions formed the mono-adduct, I(CF_2)_6CH=CISiMe_3 (5) and th...
The treatment of wool under anhydrous conditions with potassium tert-butoxide solu-tion is studied. The aim is to confine reaction to the extreme exterior off the epicuticle of the fiber and to prevent whole-fiber degradation. The results indicate thaf inter-fiber arid inter-yarn friction,tenacity and dye uptake increase,yethandle tends to be as rough as expected. And the most important thing is to keep anhydrous conditions in the treatment,
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...