Silver nitrate: Versatile reagent in organic synthesis

Abstract

(A) Silver nitrate acts as a catalyst that selectively facilitates the deprotection of trimethylsilylacetylenes under ambient conditions. Reactions are usually carried out in a homogeneous mixture of dichloromethane, water and methanol (7:1:4), to enhance the solubility of the intermediates formed during the organic transformation. Acetal, ester, benzyl and most important other silyl groups are perfectly compatible with the reaction conditions. (B) Silver nitrate mediated synthesis of pyrroles is carried out in one pot by reacting secondary vinylogous amides or carbonates with propargyl bromide. This reaction, although facile, does not generate good yields. It has been observed that functionalized pyrroles can be efficiently prepared using a two-step sequence, by propargylation of secondary enaminones using n-BuLi and propargyl bromide, followed by intramolecular hydroamination catalyzed by silver nitrate. (C) Homolytic alkylation of heteroaromatic bases, i.e substituted histidine and histamine, is carried out with the help of silver nitrate, where silver-catalyzed oxidative decarboxylation of acids by peroxydisulfate takes place. The carboxylic acid acts as a source of alkyl radical, which leads to the formation of 2,3-disubstituted L-histidine methyl ester and α-N-trifluoroacetylhistamine. (D) In a single step, silver nitrate helps in the ring enlargement of the 1-(tribromomethyl)-1,2-dihydro 1-(tribromomethyl)-1,2,3,4-tetrahydroisoquinoline derivatives to 1,2-dihydro 1,2,3,4-tetrahydrobenzo[d]azepin-2-ones, respectively, in moderate yields. Here the silver ion acts as an electrophile, which facilitates the formation of the transient aziridinium ring. The aziridium ring is opened by the methanol and the intermediate formed undergoes hydrolysis to give the desired product. (E) Alkaline silver nitrate assists in the formation of the intramolecular coupling reaction of hydroborated products formed by addition of 9-BBN and catecholborane to C-C double and triple bonds, respectively. (F) Silver nitrate assists in the conversion of aminonitrile to ketones by mild hydrolysis. In this reaction, when aqueous silver nitrate solution is added to the aminonitrile dissolved in the THF solution, rapid formation of the dark gray silver nitrate precipitate takes place and with acidic workup, one the desired product is obtained. (G) The direct introduction of a carboxyl group onto a heteroaromatic base in a single step is a very useful reaction in organic synthesis. Alkoxycarbonylation of heteroaromatic bases is carried out by silver-catalyzed decarboxylation of methyl and ethyl monoesters of oxalic acid by S2O8-. This reaction is a biphasic reaction, where monoesters are present in organic layers and protonated base is present in aqueous layer. (H) Silver nitrate catalyzes the cyclization of the allenic alcohols to form 2,5-dihydrofurans and 5,6-dihydro-2H-pyrans. To a solution of calcium carbonate and δ-monoalkyl, δ,δ-dialkyl substituted α-allenic alcohol, silver nitrate in water-dioxane or water-acetone is added to afford 2,5-dihydrofurans in 20-63% yields. Similarly, β-allenic alcohols are converted to the corresponding 5,6-dihydro-2H-pyrans under the same reaction conditions in moderate yields. (I) Homolytic alkylation of heteroaromatic bases such as quinoline is catalyzed by silver nitrate, where silver-catalyzed oxidative decarboxylation of acids by peroxydisulfate is used as a source of alkyl radical. Here, the free alkyl radical acts as a nucleophile, which attacks the protonated bases; high yields and selectivities are obtained with this reaction. © Georg Thieme Verlag Stuttgart.