Facile and environmentally benign synthetic approach to the selective mono-chlorination and mono-bromination of benzo[d]OXAZOL-2(3H)-ONES

被引:1
作者
Kurutos, Atanas [1 ]
Minkovska, Stela [2 ]
Nedialkov, Paraskev T. [3 ]
Fedorov, Yury, V [4 ]
机构
[1] Bulgarian Acad Sci, Inst Organ Chem, Ctr Phytochem, Acad G Bonchev Str,Bl 9, Sofia 1113, Bulgaria
[2] Bulgarian Acad Sci, Inst Catalysis, Sofia, Bulgaria
[3] Med Univ Sofia, Dept Pharmacognosy, Fac Pharm, Sofia, Bulgaria
[4] Russian Acad Sci, AN Nesmeyanov Inst Organoelement Cpds, Moscow, Russia
基金
俄罗斯基础研究基金会;
关键词
UREA-HYDROGEN PEROXIDE; ANTI-HIV ACTIVITY; AROMATIC-COMPOUNDS; TRIFLUOROACETIC-ANHYDRIDE; TAUTOMERIC MOBILITY; DERIVATIVES; OXIDATION; EFFICIENT; 2(3H)-BENZOXAZOLONE; BENZOXAZOLONE;
D O I
10.1002/jhet.4522
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Exhibiting a wide spectrum of practical applications, benzo[d]oxazol-2(3H)-ones (BOA) are considered as key intermediates in the synthesis of pharmaceutical products, organic dyes, and OLED materials among others. Herein, we propose an environmentally benign protocol for the selective mono-halogenation of benzo[d]oxazol-2(3H)-ones. Several chloro- and bromo-substituted BOA derivatives were prepared within less than an hour with high to excellent yields (75%-93%) via this novel, green, and energy sufficient method. This rapid and highly reproducible synthetic approach employs inexpensive commercially available urea-hydrogen peroxide complex and hydrochloric or hydrobromic acid. Simple operations and precise control over the oxidative halogenation, with water being the major by-product of the reaction outcome, are among the strong point of current facile method from the perspective of green chemistry.
引用
收藏
页码:1824 / 1831
页数:8
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