Syntheses, chemical telescoping

At the end of the synthesis reactions, the product can be pumped to another vessel or container via transfer lines. If the chemical reactions proceed to completion with negligible trace quantities of impurities, the next stage of production may commence in the same reaction vessel with addition of fresh raw materials. This process is called telescoping. 

Direct reduction of an aldehyde or ketone to the corresponding ether could potentially telescope two reactions, reduction and protection, into one step. S. Chandrasekhar of the Indian Institute of Chemical Technology, Hyderabad, reports (Tetrahedron Lett. 2004,45,5497) that in the present of polymethylhydrosiloxane (PMHS) and catalytic B(C6F,), TMS ethers of alcohols will convert aldehydes to the corresponding dialkyl ethers. The reaction works well for both saturated and benzylic alcohols. This may prove to be a useful alternative to Williamson synthesis for the preparation of complex ethers. 

Continuous microreactor systems have gained a lot of interest in the field of organic synthesis as these possess enhanced mass and heat transfer properties. Microreactor technology also offers a contemporary way of conducting chemical reactions In a more sustainable fashion due to the miniaturization and increased safety, and also In a technically improved manner due to intensified process efficiency. Recent developments in this area related to the synthesis of heterocyclic compounds are recorded in this chapter. Also, telescoping, in which several subsequent reaction steps (with or without purification) can be achieved by connecting different reactors to each other, is covered. 

The formed henzyl bromides can then potentially be used in a range of telescoped chemical transformations, including alkylations. The flow synthesis of a number of receptor ligands, using ben l bromides, has been demonstrated by Ulven. Alternatively, C-C bond coupling reactions can be performed using flow electrosynthesis, as shown in Scheme 12.6. ... 

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