Aluminum acetate triethyl

Later, it was also claimed that 3-(tetrazolyl)-4//-pyrido[ 1,2-u]pyrimidin-4-ones 159 were obtained in an one-step procedure by heating the appropriate 2-aminopyridine, ethyl (l//-tetrazol-5-yl)acetate, and triethyl orthoformate in dimethylformamide at 90°C for 1 hour, or in boiling tetra-hydrofuran for 6 hours followed by treatment with 1N potassium hydroxide at 50°C for 1 hour, or with anhydrous aluminum chloride under reflux for 6 hours (91EUP462834). 9-Methyl-3-( 1 //-tetrazolyl)-4//-pyrido[ 1,2-a]-pyrimidin-4-one 159 (R = 9-Me) could be prepared when 2-amino-3-meth-ylpyridine hydrochloride and sodium azide were suspended and stirred in dimethylformamide for 1 hour at room temperature, followed by the addition of ethyl ethoxymethylenecyanoacetate, ethoxymethylenemalo-nonitrile, ethyl cyanoacetate and triethyl orthoformate, or malononitrile and triethyl orthoformate and stirring at 90°C for 6-12 hours. Then the reaction mixture was treated with 1 N potassium hydroxide at 50°C for 1 hour, phosphoryl chloride at 90°C for 5 hours, or with concentrated hydrochloric acid at 110°C for 4 hours to give 26-62% yields. 

Next, the ethyl substituent is introduced via stepwise conversion of 12 with acetic anhydride and triethyl aluminum. This results in the completely diastereoselective formation of complex 13. The fact that the substitution of the oxygen func-... 

Attempts to convert the sulfones back into PASHs have been successful with a number of agents such as various metals (zinc, tin, magnesium, aluminum, iron, and nickel) in acetic acid, palladium on carbon with hydrazine, stannous chloride, lithium triethylborohydride, diphenylsi-lane, sodium borohydride, boron trifluoride, dicyclohexylcarbodiimide, triethyl phosphite, dimethyl dichlorosUane with lithium aluminum hydride, diphenylsilane, and triphenyl phosphine with iodine. However, none of them cleanly effect this conversion. 

In the initiation of the polymerization of vinyl chloride with triethyl-aluminum-benzoyl peroxide in the presence of allyl acetate, dibutyl ether, and pyridine, the process was thought to be a free-radical one [205, 206]. 

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