Reactions of 3,5-di-tert-butyl-1,2-benzoquinone with mercapto carboxylic acids

被引:4
作者
Ukhin, L. Yu. [1 ]
Suponitsky, K. Yu. [2 ]
Shepelenko, E. N. [3 ]
Belousova, L. V. [1 ]
Alekseenko, D. V. [1 ]
Borodkin, G. S. [1 ]
Etmetchenko, L. N. [1 ]
机构
[1] Southern Fed Univ, Inst Phys & Organ Chem, 194-2 Prosp Stachki, Rostov Na Donu 344090, Russia
[2] Russian Acad Sci, AN Nesmeyanov Inst Organoelement Cpds, 28 Ul Vavilova, Moscow 119991, Russia
[3] Russian Acad Sci, Southern Sci Ctr, 41 Ul Chekhova, Rostov Na Donu 344006, Russia
关键词
3,5-di-tert-butyl-1,2-benzoquinone; mercapto carboxylic acids; lactonization; 6,8-di-tert-butyl-9-hydroxy-3,4-dihydro-2H-1,5-benzoxathiepin-2-one; ACETIC-ACID; DERIVATIVES;
D O I
10.1007/s11172-016-1363-6
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Heating of an equimolar mixture of 3,5-di-tert-butyl-1,2-benzoquinone with thiosalicylic acid led to 2-[(4,6-di-tert-butyl-2,3-dihydroxyphenyl)thio]benzoic acid. In the case of beta-mercaptopropionic acid, 2-[(4,6-di-tert-butyl-2,3-dihydroxyphenyl)thio]propionic acid was formed, which upon reflux in Ac2O was converted to 6,8-di-tert-butyl-9-hydroxy-3,4-dihydro-2H-1,5benzoxathiepin-2-one.
引用
收藏
页码:727 / 730
页数:4
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