Selenium (W)-dichlorides 1, readily available by treatment of methyl ketones with phenylselenium trichloride or selenium tetrachloride, were treated in methylene chloride with pyridine to give a-chloroselenides 2 in a Pummerer-like reaction. Sulfuryl chloride chlorination of these materials and repeated pyridine treatment similarly afforded a, a- dichloroselenides 4.