Feist-Benary condensations1,2 to form furans are usually carried out by reacting an á-halo aldehyde and a β-keto ester under basic conditions. However, yields are often poor, and the main product is often a dihydrofuranol3 requiring subsequent acid-catalysed dehydration to form the furan. The α-halo acetaldehyde is also difficult to prepare free of water when anhydrous reaction conditions are desired.
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CAMBIE et al. (1990) studied this question.
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