130001-00-2

Upstream product

• 1772-43-6 2,4,4-trimethyl oxazoline 
• 98-88-4 benzoyl chloride 
• 98-86-2 acetophenone 

Downstream Products

• 200260-78-2 3-benzoyl-4-butyl-1-(2-hydroxy-1,1-dimethyl-ethyl)-6-phenyl-1H-pyridin-2-one 
• 200260-77-1 3-benzoyl-1-(2-hydroxy-1,1-dimethyl-ethyl)-4,6-diphenyl-1H-pyridin-2-one 
• 200260-83-9 6-benzoyl-3,3-dimethyl-7,8a-diphenyl-2,3,8,8a-tetrahydro-oxazolo[3,2-a]pyridin-5-one 
• 29261-44-7 4,6-diphenyl-2-pyridone 
• 37648-93-4 3-benzoyl-4,6-diphenylpyridin-2(1H)-one 

Relevant academic research and scientific papers

Synthesis via 2-Acylmethyl-2-oxazoline. I. A Novel Synthesis of 3-Acyl-2-pyridones by Michael Addition of 2-Acylmethyl-2-oxazoline to αβ-Acetylenic Ketones

The reaction of the sodium salt of 2-acylmethyl-4,4-dimethyl-2-oxazolines with α,β-acetylenic ketones in ethanol gave Michael adducts, which were easily transformed to 4,6-disubstituted 3-acyl-1-(2-hydroxy-1,1-dimethylethyl)-2-pyridones by silica gel. N-Dealkylation of the pyridones was performed using hydrochloric acid in good yields. Deacylation of the pyridones was performed using potassium hydroxide. A mild treatment of the pyridones with bases or silica gel gave 7-oxa-1-azabicyclo[4.3.0]non-3-en-2-one derivatives via intramolecular Michael addition. A similar reaction of 2-phenacyl-2-oxazoline with diphenylpropynone gave the corresponding 1-(2-hydroxyethyl)-2-pyridone derivative, which was inert against these 1-dealkylation, 3-deacylation, and intramolecular addition reactions.

Synthesis of Dimethyl Oxazolidine and Tetrahydro-2H-1,3-oxazine Ring Substituted Ketene N,O-Acetals

Dimethyl oxazolidine and tetrahydro-2H-1,3-oxazine ring substituted ketene N,O-acetals 3 and 4 were synthesized by the reaction of ketene S,S-acetals 2 with the corresponding amino alcohols.