40991-78-4

Basic information

• Product Name: Morpholine, 4-(oxophenylacetyl)-
• CAS NO: 40991-78-4
• Molecular Formula: C12H13NO3
• Molecular Weight: 219.24
• Mol File: 40991-78-4.mol
• Article Data: 89

Chemical Properties

• CAS DataBase Reference: Morpholine, 4-(oxophenylacetyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Morpholine, 4-(oxophenylacetyl)-(40991-78-4)
• EPA Substance Registry System: Morpholine, 4-(oxophenylacetyl)-(40991-78-4)

Safety Data

• Hazardous Substances Data: 40991-78-4(Hazardous Substances Data)

Upstream product

• 5509-99-9 2-morpholino-1-phenyl-2-thioxoethanone 
• 110-91-8 morpholine 
• 1074-12-0 phenylglyoxal hydrate 
• 4394-85-8 4-morpholinecarboxaldehyde 
• 611-73-4 Benzoylformic acid 
• 98-85-1 1-Phenylethanol 
• 109-97-7 pyrrole 
• 120-72-9 indole 
• 15206-55-0 methyl 2-oxo-2-phenylacetate 
• 591-50-4 iodobenzene 
• 201230-82-2 carbon monoxide 
• 536-74-3 phenylacetylene 
• 582-24-1 1-phenyl-2-hydroxyethanone 
• 51579-87-4 N,N-dimethyl-2-oxo-2-phenylacetamide 

Downstream Products

• 113397-16-3 (±)-7-hydroxy-7-phenyl-4-oxa-1-azabicyclo[4.2.0]octan-8-one 
• 113397-16-3 (±)-7-hydroxy-7-phenyl-4-oxa-1-azabicyclo[4.2.0]octan-8-one 
• 57872-39-6 2‐hydroxy‐1‐morpholino‐2‐phenylethan‐1‐one 

Relevant articles and documents

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The invention discloses a preparation method of an alpha-carbonyl amide compound. The method comprises the following steps: under the action of a catalyst, taking oxygen as an oxidant, and carrying out oxidative amidation reaction on an alpha-diazoketone compound shown in a chemical formula 2 and a cyclic secondary amine compound shown in a chemical formula 3 in an organic solvent to obtain the alpha-carbonyl amide compound shown in a chemical formula 1, wherein the formulas 1, 2 and 3 are also shown in the speification. According to the preparation method disclosed by the invention, the alpha-carbonyl amide compound is obtained by taking oxygen as the oxidizing agent and catalyzing alpha-diazoketone and cyclic secondary amine to be subjected to oxidative amidation reaction through cuprous iodide, the reaction condition is mild, the reaction time is short, and the byproduct of the reaction is only nitrogen, so that the method is an effective way for green and efficient preparation of the alpha-carbonyl amide compound.