CAJ | 학술논문

有机催化是催化领域的前沿.在水介质中,以水合肼作为还原剂研究了小分子有机胺催化3-甲基蒽醌-[1,2-c]-异噁唑有氧还原开环反应高效合成1-氨基-2-乙酰基蒽醌,详细考察了不同种类有机胺对异噁唑有氧还原开环反应的催化性能,发现小分子有机伯胺具有很好的还原开环催化性能.在1倍水合肼存在下室温反应3 h,3-甲基蒽醌-[1,2-c]-异噁唑转化率和目标产物1-氨基-2-乙酰基蒽醌选择性均可达到97.2%.产物的分子结构经氢核磁谱和质谱得以确证.此外,提出了小分子有机伯胺催化3-甲基蒽醌-[1,2-c]-异噁唑有氧还原开环反应合成1-氨基-2-乙酰基蒽醌的可能反应机理.
유궤최화시최화영역적전연.재수개질중,이수합정작위환원제연구료소분자유궤알최화3-갑기은곤-[1,2-c]-이오서유양환원개배반응고효합성1-안기-2-을선기은곤,상세고찰료불동충류유궤알대이오서유양환원개배반응적최화성능,발현소분자유궤백알구유흔호적환원개배최화성능.재1배수합정존재하실온반응3 h,3-갑기은곤-[1,2-c]-이오서전화솔화목표산물1-안기-2-을선기은곤선택성균가체도97.2%.산물적분자결구경경핵자보화질보득이학증.차외,제출료소분자유궤백알최화3-갑기은곤-[1,2-c]-이오서유양환원개배반응합성1-안기-2-을선기은곤적가능반응궤리.
A clean and highly efficient catalytic aerobic reductive ring‐cleavage of 3‐methylan‐thra[1,2‐c]isoxazole‐6,11‐dione to 1‐amino‐2‐acetylanthraquinone was performed using simple organic amines as organocatalysts and water as a green reaction medium. This method provides a new clean transformation of isoxazole‐containing compounds to the corresponding ortho‐amino ketones. The catalytic performance of various organic amines was carefully screened, and simple organic primary amines were found to be promising practical catalysts with outstanding catalytic performance. Isopropylamine as the organocatalyst gave 97.2% conversion of 3‐methylan‐thra[1,2‐c]isoxazole‐6,11‐dione, with 97.2% selectivity to 1‐amino‐2‐acetylanthraquinone, in the presence of oxygen only, using 1 equiv. of hydrazine hydrate at room temperature for 3 h. A possi‐ble mechanism is also proposed.