173371-56-7

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 173371-54-5 (2R,3R,5S,6S)-2,3-diethoxy-5,6-bis(hydroxymethyl)-2,3-dimethyl<1,4>dioxane 
• 173371-53-4 (2R,3R,5R,6R)-5,6-diethoxy-5,6-dimethyl<1,4>dioxane-2,3-dicarboxylic acid diethyl ester 
• 51933-13-2 3,3-Diethoxy-butan-2-one 

Relevant academic research and scientific papers

Transacetalization of Diethyl Tartrate with Acetals of α-Dicarbonyl Compounds: A Simple Access to a New Class of C2-Symmetric Auxiliaries and Ligands

A simple access to a new class of C2-symmetric auxiliaries and ligands is based on the transacetalization of diethyl tartrate (1) with monoacetals of butane-2,3-dione in the key step.Acid-catalyzed reaction of 1 with 2 equiv of 3,3-diethoxybutan-2-one (2) gives the C2-symmetric 1,4-dioxane 7 in 88percent yield.Reduction of 7 with LiAlH4 affords the crystalline diol 9.The structure of 7 was established from the X-ray structure of 9.Dioxane 7 was converted by standard methodology into the diphosphine 24 and the TARTROL 22.Reaction of 1 with 3,3-dimethoxybutan-2-one (3) in the presence of BF3-etherate gives in analogy to the formation of 7 the 1,4-dioxane 8.This compound was transformed into the diphosphine 25 and the TARTROL 23.The trans-diaxial relationship of the methoxy groups present in 8 could be deduced without X-ray analysis from the 1H-NMR spectrum of 23.