“…Generally, this purpose can be fulfilled employing methanol, methane, methyl chloride, and other C 1 resources ,, as methylation agent, among which the methanol route is the most compelling due to its low-cost nature and moderate operating conditions. Nevertheless, the main approach to the synthesis methanol is the hydrogenation of CO with hydrogen (H 2 ), wherein the CO conversion (∼10%) was strongly limited by thermodynamics leading to a high recycle ratio and energy waste. − Utilizing syngas directly as methylation agent offers an opportunity to surmount this drawback pertaining to the in situ consumption of methanol, which promotes the conversion of CO. − Briefly, acrylonitrile butadiene styrene (ABS) reaction takes place by two steps, including the transformation of syngas into methanol over metal oxides and alkylation of benzene with methanol over zeolites, as sketched in Figure S1. − The hydrogenation of CO without C–O bond cleavage has been recognized as a typical mechanism for methanol formation, while in terms of the benzene alkylation with methanol, the concerted and stepwise mechanisms are widely acceptable, though it is still quite controversial as to which route is prevailing . Besides, some side reactions like water gas shift (WGS) reaction and syngas to light hydrocarbons also exists, resulting in the formation of carbon dioxide (CO 2 ) instead of water and C 1 –C 4 products.…”