K-(Me)MoS2 catalysts (Me = Co, Fe, Ni) supported on activated carbon were synthesized via the incipient wetness impregnation method. The catalysts were characterized using low-temperature N2-adsorption, SEM-EDX, XRD, and TEM. The catalysts were evaluated in an ethanol conversion reaction using a fixed-bed reactor to investigate the influence of catalytic active phase composition on the yields of various products. It had been found that K and Co(Ni, Fe) incorporation contributed to the significant changes in catalytic behavior of sulfide catalysts. The addition of K resulted in partial poisoning of the active sites, resulting in a decrease in catalytic activity when compared to the reference MoS2/AG-3 and (Me)MoS2/AG-3 catalysts. Conversion decreased as follows: FeMoS2 > MoS2 ≥ NiMoS2 > CoMoS2 > K-CoMoS2 > K-NiMoS2 > K-MoS2 > KFeMoS2. K-addition into (Me)MoS2/AG-3 increased the yield of alcohol at the expense of acetate and hydrocarbons. It reduced the probability of C−O bond breaking in the adsorbed intermediate and altered selectivity away from alkyl fragment toward alkoxide fragment formation. This allowed us to suppose that K somewhat promotes sites responsible for higher alcohol synthesis. Catalysts free of K were shown to be more advantageous for the synthesis of ethyl acetate, resulting in high yields, particularly with the use of MoS2/AG-3 and CoMoS2/ AG-3 catalysts. © 2024 American Chemical Society.