Aniline benzaldehyde

Figure 11.2. The SHMO frontier orbitals of aniline, benzaldehyde, and styrene as prototypes of X -, Z-, and -substituted benzenes.

TRI-n-BUTYLAMINE (Table V) Aniline Benzaldehyde Miscibilities with 160 substances 43 <25 151 151 15,296(pp.404-10)... 

Keywords anilines, benzaldehydes, condensation, waste-free, azomethines... 

Butyalmine, aniline, benzaldehyde, chloroform, carbon tetrachloride, toluene, and nitrobenzene caused more than 50% reduction in tensile strength after exposure for one year. However, only butylamine, benzaldehyde, and carbon tetrachloride reduced tensile by more than 50% at three months of exposure. 

Trifluoroacetic acid, acetone, acetonitrile, acrylonitrile, aniline, benzaldehyde, m-cresol, cyclohexanone, N,N-dimethyl acetamide, N,N-dimethyl formamide, dimethyl sulfoxide, ethanol amine, formic acid, N-methyl-2-pyrolidone, nitrobenzene, propylene carbonate, pyridine, triethyl phosphate... 

Amyl Acetate Aniline Benzaldehyde Benzene Benzyl Alcohol n-fiutyl Acetate n-Butyl Alcohol n-Butyl Lactate ... 

Hydrotropes do not perform so generally as surfactants do, i.e. the solubility will not increase for all organic compounds in hydrotropic solutions. The efficacy will also vary among the different hydrotropes, even though very small structural differences may be present. This has been reported for the solubilities in aqueous sodium o-y m- and /7-xylene sulfonate solutions of solutes such as acetophenone, aniline, benzaldehyde, c7-cresol, etc. It was found that the meta structure was more effective, particularly at lower temperatures since it had a higher water solubility (5). Another example is... 

An efficient one-pot synthesis of aniUnobenzylphosphonates was achieved from the reaction of aniline, benzaldehyde, and dialkyl H-phosphonates in the presence of BF3.0Et2 as a catalyst [17],... 

The common names phenol, aniline, benzaldehyde, benzoic acid, and anisole are also retained by the lUPAC system ... 

Phenol Aniline Benzaldehyde Benzoic acid Anisole... 

Zirconium-catalyzed three-component coupling of anilines, benzaldehydes, and dihydropyranes was reported as shown in Equation 54 [59]. The reaction efficiently proceeded at room temperature in the presence of a catalytic amount of ZrCU. Since water is formed during the formation of imine from aniline and chloroben-zaldehyde, the real catalyst is probably some zirconium species derived from ZrCU and water, which is active enough for this reaction. 

Poly(methylhydroxiloxane) (PMHS) serves as the hydride source for reduction of aldehydes and ketones to alcohols with 2 mol % of the catalyst bis(dibutylacetoxytin) oxide, thus avoiding large quantities of toxic organotin hydrides. PMHS in the presence of Pd-on-charcoal in ethanol also reduces nitrobenzene to aniline, benzaldehyde to toluene, 1-alkenes to alkanes, and only the cis isomer of an isomeric mixture of 2-nonenes to nonane. 

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