77970-53-7

Basic information

• Product Name: Ethanone, 2-(ethylsulfonyl)-1-phenyl-
• Synonyms: 2-ethylsulphonylacetophenone;2-ethanesulfonyl-1-phenyl-ethanone;2-Aethansulfonyl-1-phenyl-aethanon
• CAS NO: 77970-53-7
• Molecular Formula: C10H12O3S
• Molecular Weight: 212.269
• Mol File: 77970-53-7.mol
• Article Data: 22

Chemical Properties

• CAS DataBase Reference: Ethanone, 2-(ethylsulfonyl)-1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 2-(ethylsulfonyl)-1-phenyl-(77970-53-7)
• EPA Substance Registry System: Ethanone, 2-(ethylsulfonyl)-1-phenyl-(77970-53-7)

Safety Data

• Hazardous Substances Data: 77970-53-7(Hazardous Substances Data)

Upstream product

• 10271-55-3 2-(ethylthio)-1-phenylethanone 
• 536-74-3 phenylacetylene 
• 1889-59-4 ethyl vinyl sulfone 
• 70-11-1 α-bromoacetophenone 
• 20035-08-9 sodium ethanesulfinate 
• 98-86-2 acetophenone 
• 594-44-5 Ethanesulfonyl chloride 
• 40721-68-4 N-morpholino-1-phenylethan-1-imine 
• 16717-64-9 1-azidostyrene 
• 37984-88-6 ethanesulfonic acid hydrazide 
• 100-42-5 styrene 
• 13735-81-4 1-styrenyloxytrimethylsilane 
• 19433-17-1 acetophenone O-acetyloxime 
• 2206-94-2 1-acetoxy-1-phenylethene 

Relevant articles and documents

Method for preparing beta-carbonyl sulfone compound by using half-sandwich iridium complex

The invention relates to a method for preparing a beta-carbonyl sulfone compound by using a half-sandwich iridium complex, which comprises the following step: in the presence of alkali, by taking acetophenone and sulfonyl chloride as raw materials and taking the half-sandwich iridium complex containing an o-carboborylbenzoxazole structure as a catalyst, conducting reacting at room temperature to prepare the beta-carbonyl sulfone compound. Compared with the prior art, the method has the advantages that the half-sandwich iridium complex containing the o-carboborylbenzoxazole structure is used as the catalyst, acetophenone and sulfonyl chloride are efficiently catalyzed to react under the room temperature condition to synthesize the beta-carbonyl sulfone compound, the product yield is high, the reaction condition is mild, the substrate is cheap and easy to obtain, and the catalytic efficiency is high.

Oxidative Sulfonylation of Hydrazones Enabled by Synergistic Copper/Silver Catalysis

A copper/silver-cocatalyzed protocol for oxidative sulfonylation of hydrazones is demonstrated. A wide range of β-ketosulfones and N-acylsulfonamides are directly synthesized in moderate to good yields. Our work provides a viable method for scalable preparation of β-ketosulfone derivatives that have found wide applications in the pharmaceutical industry.

Dioxygen-Triggered Oxosulfonylation/Sulfonylation of Terminal Olefins toward β-Keto Sulfones/Sulfones

A dioxygen-triggered oxosulfonylation/sulfonylation of unactivated olefins to achieve β-keto sulfones/sulfones has been developed. Interestingly, pluralistic mechanisms were found when different types of compounds were applied as substrates, and different products were achieved. The reaction is carried out with a high atomic efficiency in the absence of a metal and a catalyst at room temperature under an air atmosphere. Importantly, as a proof-of-concept, a bioactive molecule was synthesized on a gram-scale level using this method.