56308-01-1

Upstream product

• 60965-23-3 1-(ω-chloroacetyl)-2-hydroxy-4-methoxybenzene 
• 930-69-8 sodium thiophenolate 
• 56308-05-5 7-methoxy-3-(phenylthio)-4H-chromen-4-one 
• 56307-99-4 2',4'-dihydroxy-2-phenylthioacetophenone 
• 77-78-1 dimethyl sulfate 
• 108-98-5 thiophenol 

Downstream Products

• 56308-05-5 7-methoxy-3-(phenylthio)-4H-chromen-4-one 
• 153432-53-2 2-chloro-2'-hydroxy-4'-methoxy-2-(phenylthio)acetophenone 
• 153432-40-7 6-methoxy-2-phenylthiobenzofuran-3(2H)-one 

Relevant academic research and scientific papers

Arylation of α-(Phenylthio)ketones with Aryllead(IV) Derivatives: Application to the Synthesis of 2-Arylbenzofuran-3(2H)-one Derivatives

The reaction of aryllead(IV) triacetates with benzofuran-3(2H)-one 1 yields the 2,2-diarylated ketone or the monoarylated ketone with the hindered lead reagent 15. 2-Phenylthiobenzofuran-3(2H)-one 2 was easily arylated with a wide range of aryllead reagen

SYNTHESIS OF 3-PHENYLTHIOCHROMONES FROM 2'-HYDROXY-2-PHENYLTHIOACETOPHENONES

2'-Hydroxy-2-phenylthioacetophenone derivatives (4a, b) can be readily prepared either from 2'-hydroxy-2-halogenoacetophenones (1a-c) and thiophenol, or from phenylthioacetonitrile and polyphenols (route 4b, c).The partial methylation reaction of 4b is co