Activation of methane to CH3+: A selective industrial route to methanesulfonic acid

被引:62
作者
Diaz-Urrutia, Christian [1 ]
Ott, Timo [1 ]
机构
[1] Grillo Werke AG, Chem Div, R&D Dept, Weseler Str 1, D-47169 Duisburg, Germany
关键词
OXIDATION; HYDROXYLATION; HYDROCARBONS; SULFONATION; CHEMISTRY; PEROXIDE; SALTS;
D O I
10.1126/science.aav0177
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Direct methane functionalization to value-added products remains a challenge because of the propensity for overoxidation in many reaction environments. Sulfonation has emerged as an attractive approach for achieving the necessary selectivity. Here, we report a practical process for the production of methanesulfonic acid (MSA) from only two reactants: methane and sulfur trioxide. We have achieved >99% selectivity and yield of MSA. The electrophilic initiator based on a sulfonyl peroxide derivative is protonated under superacidic conditions, producing a highly electrophilic oxygen atom capable of activating a C-H bond of methane. Mechanistic studies support the formation of CH3+ as a key intermediate. This method is readily scalable with reactors connected in series for prospective production of up to 20 metric tons per year of MSA.
引用
收藏
页码:1326 / +
页数:28
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