96717-76-9Relevant articles and documents
Halogenation Using Quaternary Ammonium Polyhalides. XXXII. Dichlorination of Aromatic Acetyl Derivatives with Benzyltrimethylammonium Tetrachloroiodate
Kakinami, Takaaki,Urabe, Yasuaki,Hermawan, Irwan,Yamanishi, Hiroko,Okamoto, Tsuyoshi,Kajigaeshi, Shoji
, p. 2549 - 2551 (1992)
The reaction of aromatic acetyl derivatives with 2 molar amounts of benzyltrimethylammonium tetrachloroiodate in acetic acid at 70 deg C for several hours gave dichloroacetyl derivatives in good yields.
A convenient and efficient synthesis of 1-aryl-2,2-dichloroethanones
Terent'ev, Alexander O.,Khodykin, Sergey V.,Troitskii, Nikolay A.,Ogibin, Yuri N.,Nikishin, Gennady I.
, p. 2845 - 2848 (2007/10/03)
1-Arylethanones are readily chlorinated with an aqueous HCl-H 2O2 system using ethanol as a cosolvent. The reaction prceeds rapidly and results in selective conversion of 1-arylethanones into 1-aryl-2,2-dichloroethanones in yields of 48-89%, depending on the nature of the substituent in the aryl group.