The possibility of the selective conversion of lower alkanethiols RSH
(R = C-1-C-3) to dialkyl sulfides in the presence of the modified alum
ina catalyst was demonstrated. The corresponding symmetrical dialkyl s
ulfides were produced as a result of the alkanethiol disproportionatio
n, and the methylalkyl sulfides were produced by reactions of alkaneth
iols with methanol. The rate of the alkane methanethiol conversion cha
nged in the following order: iso-C3H7SH > C2H5SH > CH3SH. Methanethiol
quantitatively converted to dimethyl sulfide; ethanethiol and especia
lly propanethiol-2 reacted less selectively because of the decompositi
on reaction. The process is inhibited in the case of a mixture of alka
nethiols.