Benzaldehyde, diethylamine

Benzaldehyde, 4-rm-butyl-, 55, 10 Benzaldehyde, diethylamine, 58,119 Benzaldehyde, dihexylamine, 58, 119 Benzaldehyde, 3,4-dihydroxy-, 56, 48 Benzaldehyde, dimethylamire, 58, 118 BENZALDEHYDE, 4-ETHOXY-3-HY-DROXY, 56, 44... 

Plummer invented a process for the biodesulfurization of hydrocarbons [157], in which organic sulfur compounds contained in liquid hydrocarbons are converted to elemental sulfur. The reaction is carried out in the presence of a biocatalyst and hydrogen, by dissolving completely the liquid hydrocarbons in an organic solvent, such as a nucleophilic and/or electrophilic solvent(s). The nucleophilic solvent should have a pKa greater than 2, and the electrophilic solvent more negative than -2. Recommended nucleophilic solvents include -butylamine, diethylamine, butanediamine, ethylenimine, toluene, pyridine, aniline, and acetophenone. The electrophilic solvents could be methylethylketone, pyrrole, or benzaldehyde. 

High yields of bis(arylmethylidene)tetrahydrothiopyran-4-ones are achieved through a double aldol reaction of tetrahydrothiopyran-4-one with benzaldehydes in the presence of iV-(trimethylsilyl)diethylamine and LiC104 (Equation 26) <2005SL2317>. 

For example, benzylamine forms benzaldehyde products , and diethylamine is oxidised to a mixture of acetic acid, ammonia, ethanol and acetohydroxamic acid . 

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