The action of aluminum bromide on some halogenated thiophenols and benzyl phenyl sulfides
HF Wilson, DS Tarbell
Index: Wilson; Tarbell Journal of the American Chemical Society, 1950 , vol. 72, p. 5200,5203
Full Text: HTML
Citation Number: 22
Abstract
During a continuation of some investigations? on the cleavage of benzyl phenyl sulfides by aluminum bromide, it was noted that 4-bromothiophenol (I), in chlorobenzene solution containing a molar equivalent of aluminum bromide, showed a rapid disappearance of the thiol group, as determined by iodine titration. The product, which was formed in high yield, was found to be 4-chlorodiphenyl sulfide (V), and was characterized by oxidation to the ...
Related Articles:
[Bhadra, Sukalyan; Sreedhar, Bojja; Ranu, Brindaban C. Advanced Synthesis and Catalysis, 2009 , vol. 351, # 14-15 p. 2369 - 2378]
[Qian, Ding-Quan; Liu, Bo; Shine, Henry J.; Guzman-Jimenez, Ilse Y.; Whitmire, Kenton H. Journal of Physical Organic Chemistry, 2002 , vol. 15, # 3 p. 139 - 147]