• In Bischler-Napieralski synthesis, which product is formed?
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Answer:
Bischler-Napieralski Cyclization. The Bischler-Napieralski Reaction allows the synthesis of 3,4-dihydroisoquinolines from the β-ethylamides of electron-rich arenes using condensation reagents such as P2O5, POCl3 or ZnCl2.
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In Bischler-Napieralski synthesis, 3,4-dihydroisoquinolines is formed
Explanation:
- The Bischler-Napieralski Reaction uses condensation reagents to synthesise 3,4-dihydroisoquinolines from -ethylamides of electron-rich arenes.
- Fodor was able to make stable imidoyl salts at ambient temperature that produced nitrilium salts following mild heating, whereas the Bischler-Napieralski Reaction needed high temperatures to produce dihydroisoquinolines.
- As will be discussed later, a process involving nitrilium salts accounts for the appearance of styrenes as byproducts.
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