琥珀酸
酒石酸
化学
催化作用
甲基异丁基酮
有机化学
溶剂
柠檬酸
作者
Xinge Miao,Pengxin Yu,Mingzhi Du,Yongsheng Yuan,Jianyu Han,Jingen Long,Lingzhao Kong,Junju Mu,Weiran Yang
标识
DOI:10.1021/acssuschemeng.4c06345
摘要
Herein, a new method to selectively convert tartaric acid to succinic acid was developed by catalytic transfer hydrogenation using iodine as the catalyst and methyl isobutyl ketone (MIBK) as both the hydrogen donor and the solvent. Under optimized reaction conditions, 85% succinic acid can be obtained directly from tartaric acid with a catalytic amount of iodine in MIBK at 160 °C for 4 h. Moreover, succinic acid can automatically precipitate out from the reaction solvent after cooling due to its much lower solubility in MIBK at room temperature, which provides an easy way for product separation. The detailed mechanism has been studied extensively by control experiments. The cheap catalyst, mild reaction condition, and easy separation of the product make this process a green path for succinic acid production.
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