93799-43-0

Upstream product

• 6066-82-6 1-hydroxy-pyrrolidine-2,5-dione 
• 611-71-2 MANDELIC ACID 

Downstream Products

• 93823-61-1 2,2,5,5-Tetramethyl-2,5-dihydro-1H-pyrrole-3-carboxylic acid [2-(2-hydroxy-2-phenyl-acetylamino)-ethyl]-amide 
• 93823-62-2 2,2,5,5-Tetramethyl-2,5-dihydro-1H-pyrrole-3-carboxylic acid [3-(2-hydroxy-2-phenyl-acetylamino)-propyl]-amide 
• 2019-71-8 N,N-dimethyl-2-phenyl-2-hydroxyacetamide 
• 2019-69-4 N,N-diethyl-2-(2-hydroxyphenyl)acetamide 
• 110271-94-8 6-[(Z)-Benzylimino]-2-isopropoxy-5-phenyl-5,6-dihydro-[1,3,4]oxadiazine-4-carboxylic acid isopropyl ester 
• 28193-70-6 N-benzyl-2-oxo-2-phenylacetamide 
• 51579-87-4 N,N-dimethyl-2-oxo-2-phenylacetamide 
• 4410-32-6 N-benzyl-2-hydroxy-2-phenylacetamide 

Relevant academic research and scientific papers

Preparation method of N,N-diethyl-2-hydroxyl-2-phenylacetamide

The invention provides a synthesis method of N,N-diethyl-2-hydroxyl-2-phenylacetamide. The N,N-diethyl-2-hydroxyl-2-phenylacetamide is obtained by condensing mandelic acid, serving as a raw material,with N-hydroxysuccinimide, and then performing substitut

Reactions of α-Hydroxy Carbonyl Compounds with Azodicarboxylates and Triphenylphosphine: Synthesis of α-N-Hydroxy Amino Acid Derivatives

Reaction of aliphatic α-hydroxy esters with azodicarboxylates and triphenylphosphine in the presence of either CbzNHOCH2Ph or trOCNHOCH2Ph provides a direct route to protected α-N-hydroxy amino acids.Similar reactions with aromatic α-hydroxy carbonyl compounds and derivatives result in predominate oxidation to the corresponding α-oxo carbonyl derivatives.