
Chemistry of Heterocyclic Compounds p. 1301 - 1306 (1986)
Update date:2022-08-05
Topics:
Voronkov, M. G.
Deryagina, E. N.
Papernaya, L. K.
Sukhomazova, E. N.
Korchevin, N. A.
Efremova, G. G.
At 500-600 deg C, di(2-thienyl)sulfide is converted to thiophene, thiophene thiols, dithienyls, and dithienothiophenes, and isomerized to 2,3-dithienylsulfide.Hydrogen sulfide accelerates these reactions significantly.In the liquid phase the thermal conversion of di(2-thienyl)sulfide takes place only with the participation of elemental sulfur or in the system sulfur-hydrogen sulfide.Thiophene and diethienothiophenes are not formed in this case, while isomerization occurs to a large degree.The observed thermal conversions of di(2-thienyl)sulfide are based on the addition of thiyl radicals to the double bonds of the thiophene ring and to the sulfide sulfur atom.
View MoreNantong LiKai Chemical Co.,Ltd
Contact:+86-513-89068669
Address:Jincheng Science Park
Zhejiang Sucon Silicone Co.,Ltd
Contact:+86-575-88046692
Address:Qisheng Rd., Paojiang Industrial Zone, Shaoxing, Zhejiang, China.
Contact:+86-0512-88957371
Address:shanghai
Hebei Fulong Import & Export Co., Ltd.
Contact:86-311-87795661
Address:15A19 Zhongyuan Building,368 Youyi North Street,Shijiazhuang 050070,China
Xi'an Kaixiang Photoelectric Technology Co., Ltd
website:http://www.kxmaterials.com/
Contact:86-29-15991651477
Address:Building 6, Biopharmaceutical Industry R&D Cluster Base, No. 16, Caotang 4th Road, Caotang Science and Technology Industrial Base, High-tech Zone, Xi'an City, Shaanxi Province, China
Doi:10.1007/BF02496219
(1997)Doi:10.1007/BF02974939
(1999)Doi:10.1515/znb-2015-0013
(2015)Doi:10.1039/b610154b
(2006)Doi:10.1021/ja01091a051
(1965)Doi:10.1021/om9810145
(1999)